A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153632



Internal ID18854124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1495604..1496905hg38UCSC Ensembl
Outerchr10:1537799..1539100hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002287
SamplesKWB1
Known GenesADARB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153632
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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