A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519397



Internal ID15446690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:75375234..75389095hg38UCSC Ensembl
Innerchr14:75841937..75855798hg19UCSC Ensembl
Innerchr14:74911690..74925551hg18UCSC Ensembl
Innerchr14:74911690..74925551hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3813862
hg1913862
hg1813862
hg1713862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696832
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519397
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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