A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579447



Internal ID18877728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91451759..91937600hg38UCSC Ensembl
Innerchr2:91644141..92125626hg19UCSC Ensembl
Innerchr2:91007868..91489353hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38485842
hg19481486
hg18481486
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001835
Supporting Variants
Samples
Known GenesGGT8P, LOC654342
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3579447
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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