A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043508



Internal ID19132727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:62283953..62683685hg38UCSC Ensembl
Innerchr14:62750671..63150403hg19UCSC Ensembl
Innerchr14:61820424..62220156hg18UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38399733
hg19399733
hg18399733
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531053
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)nsv1043508
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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