A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054796



Internal ID19144015
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 StatusM
Merged Variants
Supporting Variantsnssv3521312
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)nsv1054796
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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