A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121355



Internal ID18929415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:136261064..136261263hg38UCSC Ensembl
Outerchr6:136582202..136582401hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3986660, nssv3965351
SamplesKWS2, KWS1
Known GenesBCLAF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121355
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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