A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516657



Internal ID15443950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9180514..9206449hg38UCSC Ensembl
Innerchr19:9291190..9317125hg19UCSC Ensembl
Innerchr19:9152190..9178125hg18UCSC Ensembl
Innerchr19:9152190..9178125hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3825936
hg1925936
hg1825936
hg1725936
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696737, nssv680084, nssv672494, nssv669934
Samples
Known GenesOR7D2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516657
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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