A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976687



Internal ID19232702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:133772575..133787422hg38UCSC Ensembl
Outerchr10:135509900..135524800hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3814848
hg1914901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124632
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976687
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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