A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154135



Internal ID19197544
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 StatusM
Merged Variants
Supporting Variantsnssv4003411
SamplesKWB1
Known GenesSEMA4D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1154135
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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