A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074963



Internal ID18978189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136261061..136261272hg38UCSC Ensembl
chr6:136582199..136582410hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765582
SamplesKWP1
Known GenesBCLAF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074963
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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