A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998962



Internal ID19186688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:160634567..160646768hg38UCSC Ensembl
Outerchr6:161055599..161067800hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3812202
hg1912202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151780
Supporting Variants
SamplesKWB1
Known GenesLPA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998962
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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