A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3505956



Internal ID18804237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:43661451..43677856hg38UCSC Ensembl
Innerchr11:43683001..43699406hg19UCSC Ensembl
Innerchr11:43639577..43655982hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3816406
hg1916406
hg1816406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039457
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)nssv3505956
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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