A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4002909



Internal ID19187741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:74424783..74429884hg38UCSC Ensembl
Outerchr9:77039699..77044800hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg385102
hg195102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151487
Supporting Variants
SamplesKWB1
Known GenesMIR6130
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4002909
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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