A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997919



Internal ID18843892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:136273185..136275532hg38UCSC Ensembl
Outerchr6:136594323..136596670hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg382348
hg192348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152883
Supporting Variants
SamplesKWB1
Known GenesBCLAF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997919
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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