A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952616



Internal ID17301490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:43167203..43168702hg38UCSC Ensembl
Outerchr15:43459401..43460900hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999083
SamplesBILGI_BIOE
Known GenesTMEM62
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952616
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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