nsv5428185

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,704

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 genomic11,937,064-11,939,767Question Mark
Overlapping variant regions from other studies: 126 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):11,997,121-11,999,824Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5428185Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr111,937,06411,939,767
nsv5428185RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr111,997,12111,999,824

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16893163deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16893163Submitted genomicNC_000001.11:g.119
37064_11939767del
GRCh38 (hg38)NC_000001.11Chr111,937,06411,939,767
nssv16893163RemappedPerfectNC_000001.10:g.119
97121_11999824del
GRCh37.p13First PassNC_000001.10Chr111,997,12111,999,824

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)
nssv16893163<0.00126404
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