A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960993



Internal ID19215993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:35577467..35582139hg38UCSC Ensembl
Outerchr10:35866395..35871067hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg384673
hg194673
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120215
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960993
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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