A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704362



Internal ID15094328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:118610716..118657714hg38UCSC Ensembl
Innerchr11:118481431..118528424hg19UCSC Ensembl
Innerchr11:117986641..118033634hg18UCSC Ensembl
Innerchr11:117986641..118033634hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3846999
hg1946994
hg1846994
hg1746994
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527864
Supporting Variants
Samples
Known GenesMIR6716, PHLDB1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704362
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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