U.S. flag

An official website of the United States government

nsv5435509

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,166,451

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2244 SVs from 108 studies. See in: genome view    
Submitted genomic109,743,550-110,910,000Question Mark
Overlapping variant regions from other studies: 2244 SVs from 108 studies. See in: genome view    
Remapped(Score: Perfect):110,501,127-111,667,577Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5435509Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2109,743,550110,910,000
nsv5435509RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2110,501,127111,667,577

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16917230duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16917230Submitted genomicNC_000002.12:g.109
743550_110910000du
p
GRCh38 (hg38)NC_000002.12Chr2109,743,550110,910,000
nssv16917230RemappedPerfectNC_000002.11:g.110
501127_111667577du
p
GRCh37.p13First PassNC_000002.11Chr2110,501,127111,667,577

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)
nssv16917230<0.00126398
Support Center