A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703528



Internal ID15440180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:45279043..45314343hg38UCSC Ensembl
Innerchr14:45748246..45783546hg19UCSC Ensembl
Innerchr14:44817996..44853296hg18UCSC Ensembl
Innerchr14:44817996..44853296hg17UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3835301
hg1935301
hg1835301
hg1735301
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527140
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703528
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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