A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693620



Internal ID15083586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5306824..5318770hg38UCSC Ensembl
Innerchr9:5306824..5318770hg19UCSC Ensembl
Innerchr9:5296824..5308770hg18UCSC Ensembl
Innerchr9:5296824..5308770hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3811947
hg1911947
hg1811947
hg1711947
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516752
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693620
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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