A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005314



Internal ID18747845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24649201..24772469hg38UCSC Ensembl
Innerchr3:24690692..24813960hg19UCSC Ensembl
Innerchr3:24665696..24788964hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38123269
hg19123269
hg18123269
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589501
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)nsv1005314
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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