A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704435



Internal ID15441087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84738464..84837504hg38UCSC Ensembl
Innerchr11:84449507..84548547hg19UCSC Ensembl
Innerchr11:84127155..84226195hg18UCSC Ensembl
Innerchr11:84127155..84226195hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3899041
hg1999041
hg1899041
hg1799041
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527928
Supporting Variants
Samples
Known GenesDLG2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704435
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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