U.S. flag

An official website of the United States government

nsv5564056

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 70 SVs from 16 studies. See in: genome view    
Submitted genomic153,597,424-153,597,475Question Mark
Overlapping variant regions from other studies: 70 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):152,976,984-152,977,035Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5564056Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5153,597,424153,597,475
nsv5564056RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5152,976,984152,977,035

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16976346line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16976346Submitted genomicNC_000005.10:g.153
597424_153597475in
s6019
GRCh38 (hg38)NC_000005.10Chr5153,597,424153,597,475
nssv16976346RemappedPerfectNC_000005.9:g.1529
76984_152977035ins
6019
GRCh37.p13First PassNC_000005.9Chr5152,976,984152,977,035

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)
nssv16976346<0.00126402
Support Center