A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703145



Internal ID15439797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101455553..101465088hg38UCSC Ensembl
Innerchr14:101921890..101931425hg19UCSC Ensembl
Innerchr14:100991643..101001178hg18UCSC Ensembl
Innerchr14:100991643..101001178hg17UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg389536
hg199536
hg189536
hg179536
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526792
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703145
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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