A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4001899



Internal ID19194874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:63912265..63918366hg38UCSC Ensembl
Outerchr9:68507999..68514100hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg386102
hg196102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150963
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4001899
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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