A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697122



Internal ID15087088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86299747..86302319hg38UCSC Ensembl
Innerchr11:86010789..86013361hg19UCSC Ensembl
Innerchr11:85688437..85691009hg18UCSC Ensembl
Innerchr11:85688437..85691009hg17UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg382573
hg192573
hg182573
hg172573
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519914
Supporting Variants
Samples
Known GenesC11orf73
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697122
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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