A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979208



Internal ID19235979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:42097572..42104802hg38UCSC Ensembl
Outerchr10:42596699..42600250hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg387231
hg193552
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116644
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979208
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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