A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678684



Internal ID15415336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:114641293..114641905hg38UCSC Ensembl
Innerchr11:114512015..114512627hg19UCSC Ensembl
Innerchr11:114017225..114017837hg18UCSC Ensembl
Innerchr11:114017225..114017837hg17UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38613
hg19613
hg18613
hg17613
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517300
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678684
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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