A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961028



Internal ID19222628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:54536218..54547152hg38UCSC Ensembl
Outerchr11:51572128..51583062hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3810935
hg1910935
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120244
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961028
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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