nsv5642515

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 126 SVs from 22 studies. See in: genome view    
Submitted genomic59,092,275-59,092,275Question Mark
Overlapping variant regions from other studies: 126 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):60,004,834-60,004,834Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5642515Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr859,092,27559,092,275
nsv5642515RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr860,004,83460,004,834

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17156423insertionHG03486SequencingSequence alignment4,355
nssv17158102insertionSAMN00006466SequencingSequence alignment4,625

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17156423Submitted genomicNC_000008.11:g.590
92275_59092276ins2
89		GRCh38 (hg38)NC_000008.11Chr859,092,27559,092,275
nssv17158102Submitted genomicNC_000008.11:g.590
92275_59092276ins6
83		GRCh38 (hg38)NC_000008.11Chr859,092,27559,092,275
nssv17156423RemappedPerfectNC_000008.10:g.600
04834_60004835ins2
89		GRCh37.p13First PassNC_000008.10Chr860,004,83460,004,834
nssv17158102RemappedPerfectNC_000008.10:g.600
04834_60004835ins6
83		GRCh37.p13First PassNC_000008.10Chr860,004,83460,004,834

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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