A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124119



Internal ID18919551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:136269611..136271993hg38UCSC Ensembl
Outerchr6:136590749..136593131hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg382383
hg192383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975434
SamplesKWS2
Known GenesBCLAF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124119
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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