A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3577052



Internal ID18875333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13708814..13815503hg38UCSC Ensembl
Innerchr2:13848939..13955628hg19UCSC Ensembl
Innerchr2:13766390..13873079hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38106690
hg19106690
hg18106690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008170
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)nssv3577052
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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