A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070037



Internal ID19325560
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 StatusM
Merged Variants
Supporting Variantsnssv3762887
SamplesKWP1
Known GenesCTNND1, TMX2-CTNND1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070037
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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