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nsv5497884

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:680

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 90 SVs from 26 studies. See in: genome view    
Submitted genomic116,870,772-116,871,451Question Mark
Overlapping variant regions from other studies: 90 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):117,308,577-117,309,256Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5497884Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12116,870,772116,871,451
nsv5497884RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12117,308,577117,309,256

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17684720deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17684720Submitted genomicNC_000012.12:g.116
870772_116871451de
l
GRCh38 (hg38)NC_000012.12Chr12116,870,772116,871,451
nssv17684720RemappedPerfectNC_000012.11:g.117
308577_117309256de
l
GRCh37.p13First PassNC_000012.11Chr12117,308,577117,309,256

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)
nssv176847200.00196392
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