A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146486



Internal ID19196458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:160612567..160633768hg38UCSC Ensembl
Outerchr6:161033599..161054800hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3821202
hg1921202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3995640
SamplesKWB1
Known GenesLPA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146486
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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