A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150640



Internal ID19202595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:22553496..22556697hg38UCSC Ensembl
Outerchr15:23316399..23319600hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg383202
hg193202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996114
SamplesKWB1
Known GenesHERC2P2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150640
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer