A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153665



Internal ID19200460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:101623371..101624772hg38UCSC Ensembl
Outerchr8:102635599..102637000hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002321
SamplesKWB1
Known GenesGRHL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153665
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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