A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151763



Internal ID19201682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:45669662..45674363hg38UCSC Ensembl
Outerchr6:45637399..45642100hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg384702
hg194702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998945
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151763
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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