A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132392



Internal ID19267967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:20162147..20423147hg38UCSC Ensembl
Outerchr15:20367400..20628400hg19UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38261001
hg19261001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987167
SamplesKWS1
Known GenesCHEK2P2, HERC2P3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132392
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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