U.S. flag

An official website of the United States government

nsv5507855

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:280

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 94 SVs from 15 studies. See in: genome view    
Submitted genomic113,807,681-113,807,960Question Mark
Overlapping variant regions from other studies: 94 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):113,678,403-113,678,682Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5507855Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11113,807,681113,807,960
nsv5507855RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11113,678,403113,678,682

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17052479deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17052479Submitted genomicNC_000011.10:g.113
807681_113807960de
l
GRCh38 (hg38)NC_000011.10Chr11113,807,681113,807,960
nssv17052479RemappedPerfectNC_000011.9:g.1136
78403_113678682del
GRCh37.p13First PassNC_000011.9Chr11113,678,403113,678,682

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)
nssv17052479<0.00116404
Support Center