A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698726



Internal ID15435378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:97773192..97807012hg38UCSC Ensembl
Innerchr14:98239529..98273349hg19UCSC Ensembl
Innerchr14:97309282..97343102hg18UCSC Ensembl
Innerchr14:97309282..97343102hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3833821
hg1933821
hg1833821
hg1733821
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523043
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698726
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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