A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979154



Internal ID19231525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:33095433..33095535hg38UCSC Ensembl
Outerchr10:33384361..33384463hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140447
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979154
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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