A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952312



Internal ID17301186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:20384348..20422947hg38UCSC Ensembl
Outerchr15:20589601..20628200hg19UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3838600
hg1938600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999000
SamplesBILGI_BIOE
Known GenesHERC2P3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952312
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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