A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959461



Internal ID19219876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:2123770..2126370hg38UCSC Ensembl
Outerchr11:2145000..2147600hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382601
hg192601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110193
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959461
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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