A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517884



Internal ID15445177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:61125908..61146788hg38UCSC Ensembl
Innerchr14:61592626..61613506hg19UCSC Ensembl
Innerchr14:60662379..60683259hg18UCSC Ensembl
Innerchr14:60662379..60683259hg17UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3820881
hg1920881
hg1820881
hg1720881
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695293
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517884
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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