A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696229



Internal ID15432881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:46052891..46059551hg38UCSC Ensembl
Innerchr14:46522094..46528754hg19UCSC Ensembl
Innerchr14:45591844..45598504hg18UCSC Ensembl
Innerchr14:45591844..45598504hg17UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg386661
hg196661
hg186661
hg176661
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516946
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696229
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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