A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980030



Internal ID19241038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:159604763..159604854hg38UCSC Ensembl
Outerchr6:160025795..160025886hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143166
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980030
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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