A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679295



Internal ID15415947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89701126..89724220hg38UCSC Ensembl
Innerchr14:90167470..90190564hg19UCSC Ensembl
Innerchr14:89237223..89260317hg18UCSC Ensembl
Innerchr14:89237223..89260317hg17UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3823095
hg1923095
hg1823095
hg1723095
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517465
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679295
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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