A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149618



Internal ID19201042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:64682142..64685143hg38UCSC Ensembl
Outerchr8:65594699..65597700hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg383002
hg193002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000920
SamplesKWB1
Known GenesCYP7B1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149618
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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