A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071054



Internal ID18973081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111405695..111406296hg38UCSC Ensembl
chr12:111843499..111844100hg19UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769955
SamplesKWP1
Known GenesSH2B3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071054
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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