U.S. flag

An official website of the United States government

nsv5520745

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26,602

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 299 SVs from 52 studies. See in: genome view    
Submitted genomic70,247,722-70,274,323Question Mark
Overlapping variant regions from other studies: 299 SVs from 52 studies. See in: genome view    
Remapped(Score: Perfect):70,281,625-70,308,226Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5520745Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1670,247,72270,274,323
nsv5520745RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1670,281,62570,308,226

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17707186duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17707186Submitted genomicNC_000016.10:g.702
47722_70274323dup
GRCh38 (hg38)NC_000016.10Chr1670,247,72270,274,323
nssv17707186RemappedPerfectNC_000016.9:g.7028
1625_70308226dup
GRCh37.p13First PassNC_000016.9Chr1670,281,62570,308,226

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)
nssv17707186<0.00126404
Support Center