A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506463



Internal ID18804744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97344008..97428447hg38UCSC Ensembl
Innerchr11:97215008..97299447hg19UCSC Ensembl
Innerchr11:96720218..96804657hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3884440
hg1984440
hg1884440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042188
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)nssv3506463
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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