A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152099



Internal ID19197686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:30366496..30368097hg38UCSC Ensembl
Outerchr15:30658699..30660300hg19UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999651
SamplesKWB1
Known GenesCHRFAM7A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152099
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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