A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3995794



Internal ID19189056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:10691236..10695237hg38UCSC Ensembl
Outerchr10:10733199..10737200hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg384002
hg194002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146639
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3995794
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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