A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585696



Internal ID18883977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:215706919..215739740hg38UCSC Ensembl
Innerchr2:216571642..216604463hg19UCSC Ensembl
Innerchr2:216279887..216312708hg18UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3832822
hg1932822
hg1832822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011860
Supporting Variants
Samples
Known GenesLINC00607
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3585696
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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