A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3521312



Internal ID18819593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54880568..55021565hg38UCSC Ensembl
Innerchr11:51095992..51238712hg19UCSC Ensembl
Innerchr11:50952568..51095288hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38140998
hg19142721
hg18142721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054796
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3521312
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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