A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3581686



Internal ID18879967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:51039660..51188856hg38UCSC Ensembl
Innerchr2:51266798..51415994hg19UCSC Ensembl
Innerchr2:51120302..51269498hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38149197
hg19149197
hg18149197
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012208
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)nssv3581686
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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