A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762943



Internal ID19309981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34209352..34209953hg38UCSC Ensembl
chr11:34230899..34231500hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070020
Supporting Variants
SamplesKWP1
Known GenesABTB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762943
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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