A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519702



Internal ID15446995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:98857675..98870750hg38UCSC Ensembl
Innerchr14:99324012..99337087hg19UCSC Ensembl
Innerchr14:98393765..98406840hg18UCSC Ensembl
Innerchr14:98393765..98406840hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3813076
hg1913076
hg1813076
hg1713076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv657659, nssv672618
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519702
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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