A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698307



Internal ID15434959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28646910..28649036hg38UCSC Ensembl
Innerchr14:29116116..29118242hg19UCSC Ensembl
Innerchr14:28185867..28187993hg18UCSC Ensembl
Innerchr14:28185867..28187993hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg382127
hg192127
hg182127
hg172127
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521687
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698307
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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