A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146202



Internal ID18854237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:515639..515756hg38UCSC Ensembl
Outerchr6:515639..515756hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999406
SamplesKWB1
Known GenesEXOC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146202
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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