A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762887



Internal ID19308452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57807220..57809220hg38UCSC Ensembl
chr11:57574692..57576692hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg382001
hg192001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070037
Supporting Variants
SamplesKWP1
Known GenesCTNND1, TMX2-CTNND1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762887
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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