A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963761



Internal ID18874679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:106709973..106710054hg38UCSC Ensembl
Outerchr11:106580699..106580780hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129523
Supporting Variants
SamplesKWS1
Known GenesGUCY1A2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963761
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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