A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751263



Internal ID18378823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58620713..58620962hg38UCSC Ensembl
Outerchr15:58620651..58620979hg38UCSC Ensembl
Innerchr15:58912912..58913161hg19UCSC Ensembl
Outerchr15:58912850..58913178hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552516
Supporting Variants
Samples
Known GenesADAM10
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751263
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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