A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698584



Internal ID15088550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:48228393..48237743hg38UCSC Ensembl
Innerchr15:48520590..48529940hg19UCSC Ensembl
Innerchr15:46307882..46317232hg18UCSC Ensembl
Innerchr15:46307882..46317232hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg389351
hg199351
hg189351
hg179351
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522923
Supporting Variants
Samples
Known GenesSLC12A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698584
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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