A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699590



Internal ID15089556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29119123..29120363hg38UCSC Ensembl
Innerchr15:29411326..29412566hg19UCSC Ensembl
Innerchr15:27198618..27199858hg18UCSC Ensembl
Innerchr15:27198618..27199858hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381241
hg191241
hg181241
hg171241
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515798
Supporting Variants
Samples
Known GenesFAM189A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699590
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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