A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663411



Internal ID15053377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18606871..18622211hg38UCSC Ensembl
Innerchr11:18628418..18643758hg19UCSC Ensembl
Innerchr11:18584994..18600334hg18UCSC Ensembl
Innerchr11:18584994..18600334hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3815341
hg1915341
hg1815341
hg1715341
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516413
Supporting Variants
Samples
Known GenesSPTY2D1, SPTY2D1-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663411
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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