A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966014



Internal ID18897709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:136261510..136268162hg38UCSC Ensembl
Outerchr6:136582648..136589300hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg386653
hg196653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130109
Supporting Variants
SamplesKWS2
Known GenesBCLAF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966014
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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