A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521740



Internal ID15449033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42385220..42441481hg38UCSC Ensembl
Innerchr14:42854423..42910684hg19UCSC Ensembl
Innerchr14:41924173..41980434hg18UCSC Ensembl
Innerchr14:41924173..41980434hg17UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3856262
hg1956262
hg1856262
hg1756262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694093
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521740
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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