U.S. flag

An official website of the United States government

nsv5502555

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,928

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 159 SVs from 41 studies. See in: genome view    
Submitted genomic121,161,634-121,164,561Question Mark
Overlapping variant regions from other studies: 158 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):121,599,437-121,602,364Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5502555Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12121,161,634121,164,561
nsv5502555RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12121,599,437121,602,364

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17684965deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17684965Submitted genomicNC_000012.12:g.121
161634_121164561de
l
GRCh38 (hg38)NC_000012.12Chr12121,161,634121,164,561
nssv17684965RemappedPerfectNC_000012.11:g.121
599437_121602364de
l
GRCh37.p13First PassNC_000012.11Chr12121,599,437121,602,364

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)
nssv17684965<0.00136404
Support Center