A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3688886



Internal ID18987167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:35209766..35356688hg38UCSC Ensembl
Innerchr9:35209763..35356685hg19UCSC Ensembl
Innerchr9:35199763..35346685hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38146923
hg19146923
hg18146923
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025195
Supporting Variants
Samples
Known GenesUNC13B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3688886
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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