A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525304



Internal ID15105911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93096738..93144367hg38UCSC Ensembl
Innerchr11:92829904..92877533hg19UCSC Ensembl
Innerchr11:92469552..92517181hg18UCSC Ensembl
Innerchr11:92469552..92517181hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3847630
hg1947630
hg1847630
hg1747630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701410
Samples
Known GenesSLC36A4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525304
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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