A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976688



Internal ID18899962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:104000..196800hg38UCSC Ensembl
Outerchr11:104000..196800hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3892801
hg1992801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124633
Supporting Variants
SamplesKWS2
Known GenesLINC01001, LOC653486, ODF3, SCGB1C1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976688
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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