A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959698



Internal ID19212817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:67055741..67216441hg38UCSC Ensembl
Outerchr9:40476400..40637100hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38160701
hg19160701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119262
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959698
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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