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nsv5465077

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,984

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 101 SVs from 19 studies. See in: genome view    
Submitted genomic149,631,460-149,633,443Question Mark
Overlapping variant regions from other studies: 101 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):149,011,023-149,013,006Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5465077Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5149,631,460149,633,443
nsv5465077RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5149,011,023149,013,006

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16975644deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16975644Submitted genomicNC_000005.10:g.149
631460_149633443de
l
GRCh38 (hg38)NC_000005.10Chr5149,631,460149,633,443
nssv16975644RemappedPerfectNC_000005.9:g.1490
11023_149013006del
GRCh37.p13First PassNC_000005.9Chr5149,011,023149,013,006

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16975644<0.00126404
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