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nsv4053204

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:54

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 33 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):154,960,693-154,960,746Question Mark
Overlapping variant regions from other studies: 35 SVs from 6 studies. See in: genome view    
Submitted genomic154,933,169-154,933,222Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4053204RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1154,960,693154,960,746
nsv4053204Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr1154,933,169154,933,222

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15854526deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15854526RemappedPerfectNC_000001.11:g.154
960693_154960746de
l
GRCh38.p12First PassNC_000001.11Chr1154,960,693154,960,746
nssv15854526Submitted genomicNC_000001.10:g.154
933169_154933222de
l
GRCh37.p13NC_000001.10Chr1154,933,169154,933,222

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)
nssv158545264.6e-005121692
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