U.S. flag

An official website of the United States government

nsv5468757

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,835

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 100 SVs from 19 studies. See in: genome view    
Submitted genomic179,751,170-179,753,004Question Mark
Overlapping variant regions from other studies: 100 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):179,178,171-179,180,005Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5468757Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5179,751,170179,753,004
nsv5468757RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5179,178,171179,180,005

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16979768duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16979768Submitted genomicNC_000005.10:g.179
751170_179753004du
p
GRCh38 (hg38)NC_000005.10Chr5179,751,170179,753,004
nssv16979768RemappedPerfectNC_000005.9:g.1791
78171_179180005dup
GRCh37.p13First PassNC_000005.9Chr5179,178,171179,180,005

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)
nssv16979768<0.00166402
Support Center