A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699329



Internal ID15435981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:36810511..36811284hg38UCSC Ensembl
Innerchr14:37279716..37280489hg19UCSC Ensembl
Innerchr14:36349467..36350240hg18UCSC Ensembl
Innerchr14:36349467..36350240hg17UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38774
hg19774
hg18774
hg17774
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523551
Supporting Variants
Samples
Known GenesSLC25A21
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699329
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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