A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003433



Internal ID19193844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:65244693..65258194hg38UCSC Ensembl
Outerchr9:70138299..70151800hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3813502
hg1913502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150130
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003433
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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