A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9750968



Internal ID18725214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25686312..25687215hg38UCSC Ensembl
Outerchr15:25686159..25687298hg38UCSC Ensembl
Innerchr15:25931459..25932362hg19UCSC Ensembl
Outerchr15:25931306..25932445hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381140
hg191140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552221
Supporting Variants
Samples
Known GenesATP10A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9750968
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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