A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710611



Internal ID19008892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61991088..62108238hg38UCSC Ensembl
Innerchr11:61758560..61875710hg19UCSC Ensembl
Innerchr11:61515136..61632286hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38117151
hg19117151
hg18117151
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053479
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)nssv3710611
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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