A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952618



Internal ID17301492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:45460403..45468602hg38UCSC Ensembl
Outerchr15:45752601..45760800hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg388200
hg198200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999085
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952618
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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