A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980408



Internal ID19244425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:15984100..15984189hg38UCSC Ensembl
Outerchr9:15984098..15984187hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143222
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980408
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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