A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3517228



Internal ID18468823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76436041..76556073hg38UCSC Ensembl
Innerchr11:76147085..76267117hg19UCSC Ensembl
Innerchr11:75824733..75944765hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38120033
hg19120033
hg18120033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050713
Supporting Variants
Samples
Known GenesC11orf30
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3517228
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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