A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660889



Internal ID15397541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34647083..34648939hg38UCSC Ensembl
Innerchr14:35116289..35118145hg19UCSC Ensembl
Innerchr14:34186040..34187896hg18UCSC Ensembl
Innerchr14:34186040..34187896hg17UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg381857
hg191857
hg181857
hg171857
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516595
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660889
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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