A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691186



Internal ID15081152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84909589..84911423hg38UCSC Ensembl
Innerchr15:85452820..85454654hg19UCSC Ensembl
Innerchr15:83253824..83255658hg18UCSC Ensembl
Innerchr15:83253824..83255658hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg381835
hg191835
hg181835
hg171835
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519285
Supporting Variants
Samples
Known GenesSLC28A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691186
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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