A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003411



Internal ID19192356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:89368084..89370685hg38UCSC Ensembl
Outerchr9:91982999..91985600hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg382602
hg192602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154135
Supporting Variants
SamplesKWB1
Known GenesSEMA4D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003411
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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