A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579426



Internal ID18877707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91426526..91627676hg38UCSC Ensembl
Innerchr2:91618895..91815702hg19UCSC Ensembl
Innerchr2:90982622..91179429hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38201151
hg19196808
hg18196808
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008010
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)nssv3579426
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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