A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769246



Internal ID18959828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34483352..34484553hg38UCSC Ensembl
chr11:34504899..34506100hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075830
Supporting Variants
SamplesKWP1
Known GenesELF5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769246
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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