A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669934



Internal ID15406586
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 StatusS
Merged Variantsnsv516657
Supporting Variants
Samples
Known GenesOR7D2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669934
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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