A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526260



Internal ID15453553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42028828..42203207hg38UCSC Ensembl
Innerchr14:42498031..42672410hg19UCSC Ensembl
Innerchr14:41567781..41742160hg18UCSC Ensembl
Innerchr14:41567781..41742160hg17UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38174380
hg19174380
hg18174380
hg17174380
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702532
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526260
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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