A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997202



Internal ID19188425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:28557953..28665454hg38UCSC Ensembl
Outerchr15:28803099..28910600hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38107502
hg19107502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145837
Supporting Variants
SamplesKWB1
Known GenesHERC2P9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997202
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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