A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976668



Internal ID19226685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:35859172..35864872hg38UCSC Ensembl
Outerchr10:36148100..36153800hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg385701
hg195701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124614
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976668
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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