A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3996483



Internal ID19190312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:168309367..168309446hg38UCSC Ensembl
Outerchr6:168710047..168710126hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1147693
Supporting Variants
SamplesKWB1
Known GenesDACT2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3996483
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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