A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147836



Internal ID19195131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:93110030..93114423hg38UCSC Ensembl
Outerchr6:93819748..93824141hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg384394
hg194394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996623
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147836
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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