A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4002092



Internal ID19192403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:67327880..67329278hg38UCSC Ensembl
Outerchr9:40062799..40064200hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg381399
hg191402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151155
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4002092
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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