A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585682



Internal ID18883963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:214593909..214636431hg38UCSC Ensembl
Innerchr2:215458633..215501155hg19UCSC Ensembl
Innerchr2:215166878..215209400hg18UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3842523
hg1942523
hg1842523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011635
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)nssv3585682
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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