U.S. flag

An official website of the United States government

nsv5547905

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:31

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 111 SVs from 26 studies. See in: genome view    
Submitted genomic81,960,289-81,960,319Question Mark
Overlapping variant regions from other studies: 111 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):82,354,068-82,354,098Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5547905Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1281,960,28981,960,319
nsv5547905RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1282,354,06882,354,098

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17689541insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17689541Submitted genomicNC_000012.12:g.819
60289_81960319ins8
5
GRCh38 (hg38)NC_000012.12Chr1281,960,28981,960,319
nssv17689541RemappedPerfectNC_000012.11:g.823
54068_82354098ins8
5
GRCh37.p13First PassNC_000012.11Chr1282,354,06882,354,098

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)
nssv17689541<0.00116404
Support Center