A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701578



Internal ID15438230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:115516731..115542275hg38UCSC Ensembl
Innerchr11:115387449..115412993hg19UCSC Ensembl
Innerchr11:114892659..114918203hg18UCSC Ensembl
Innerchr11:114892659..114918203hg17UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3825545
hg1925545
hg1825545
hg1725545
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525450
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701578
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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