A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145967



Internal ID18852353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:57436701..60346451hg38UCSC Ensembl
Outerchr6:57301499..57318300hg19UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg382909751
hg1916802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997331
SamplesKWB1
Known GenesPRIM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1145967
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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