A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661651



Internal ID15051617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:46613802..46948944hg38UCSC Ensembl
Innerchr14:47083005..47418147hg19UCSC Ensembl
Innerchr14:46152755..46487897hg18UCSC Ensembl
Innerchr14:46152755..46487897hg17UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38335143
hg19335143
hg18335143
hg17335143
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517764
Supporting Variants
Samples
Known GenesMDGA2, RPL10L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661651
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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