A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002436



Internal ID19091653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:30994731..31044060hg38UCSC Ensembl
Innerchr3:31036223..31085552hg19UCSC Ensembl
Innerchr3:31011227..31060556hg18UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg3849330
hg1949330
hg1849330
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739670
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)nsv1002436
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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