A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959060



Internal ID19203924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:22553596..22558896hg38UCSC Ensembl
Outerchr15:23314200..23319500hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg385301
hg195301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118550
Supporting Variants
SamplesKWS1
Known GenesHERC2P2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959060
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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