A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3988427



Internal ID19210070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:35914283..35914398hg38UCSC Ensembl
Outerchr9:35914280..35914395hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134922
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3988427
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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