A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001863



Internal ID18744394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:202325740..202362042hg38UCSC Ensembl
Innerchr2:203190463..203226765hg19UCSC Ensembl
Innerchr2:202898708..202935010hg18UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3836303
hg1936303
hg1836303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3583992
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)nsv1001863
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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