A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703792



Internal ID15440444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:75957591..76043576hg38UCSC Ensembl
Innerchr11:75668635..75754620hg19UCSC Ensembl
Innerchr11:75346283..75432268hg18UCSC Ensembl
Innerchr11:75346283..75432268hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3885986
hg1985986
hg1885986
hg1785986
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515973
Supporting Variants
Samples
Known GenesUVRAG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703792
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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