A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987989



Internal ID19210053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:41858058..41884831hg38UCSC Ensembl
Outerchr10:42355378..42382151hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3826774
hg1926774
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133150
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987989
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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