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nsv5427806

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:49,208

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 254 SVs from 39 studies. See in: genome view    
Submitted genomic179,716,874-179,766,081Question Mark
Overlapping variant regions from other studies: 256 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):179,686,009-179,735,216Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5427806Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1179,716,874179,766,081
nsv5427806RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1179,686,009179,735,216

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16892330duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16892330Submitted genomicNC_000001.11:g.179
716874_179766081du
p
GRCh38 (hg38)NC_000001.11Chr1179,716,874179,766,081
nssv16892330RemappedPerfectNC_000001.10:g.179
686009_179735216du
p
GRCh37.p13First PassNC_000001.10Chr1179,686,009179,735,216

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)
nssv16892330<0.00136404
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