A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137154



Internal ID18939130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:136276506..136277862hg38UCSC Ensembl
Outerchr6:136597644..136599000hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg381357
hg191357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975842
SamplesKWS2
Known GenesBCLAF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137154
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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