A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952613



Internal ID16954800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41816803..41884902hg38UCSC Ensembl
Outerchr15:42109001..42177100hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3868100
hg1968100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999080
SamplesBILGI_BIOE
Known GenesJMJD7, JMJD7-PLA2G4B, MAPKBP1, MIR4310, PLA2G4B, SPTBN5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952613
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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