A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705617



Internal ID15442269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:83912025..83924047hg38UCSC Ensembl
Innerchr14:84378369..84390391hg19UCSC Ensembl
Innerchr14:83448122..83460144hg18UCSC Ensembl
Innerchr14:83448122..83460144hg17UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3812023
hg1912023
hg1812023
hg1712023
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528927
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705617
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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