A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3501107



Internal ID19088748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:118431001..118505558hg38UCSC Ensembl
Innerchr1:118973624..119048181hg19UCSC Ensembl
Innerchr1:118775147..118849704hg18UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3874558
hg1974558
hg1874558
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001757
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3501107
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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