A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025195



Internal ID19114413
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 StatusM
Merged Variants
Supporting Variantsnssv3688886
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)nsv1025195
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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