A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952614



Internal ID16954801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:42139503..42164202hg38UCSC Ensembl
Outerchr15:42431701..42456400hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3824700
hg1924700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999081
SamplesBILGI_BIOE
Known GenesPLA2G4F, VPS39
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952614
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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