A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585681



Internal ID18883962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:214593909..214631740hg38UCSC Ensembl
Innerchr2:215458633..215496464hg19UCSC Ensembl
Innerchr2:215166878..215204709hg18UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3837832
hg1937832
hg1837832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998532
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)nssv3585681
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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