A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960638



Internal ID19209991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:28595754..28675154hg38UCSC Ensembl
Outerchr15:28840900..28920300hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3879401
hg1979401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128725
Supporting Variants
SamplesKWS1
Known GenesHERC2P9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960638
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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