A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999535



Internal ID18846364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:33385001..33389902hg38UCSC Ensembl
Outerchr9:33384999..33389900hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg384902
hg194902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146331
Supporting Variants
SamplesKWB1
Known GenesAQP7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999535
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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