A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751308



Internal ID18725554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:64340994..64341296hg38UCSC Ensembl
Outerchr15:64340927..64341344hg38UCSC Ensembl
Innerchr15:64633193..64633495hg19UCSC Ensembl
Outerchr15:64633126..64633543hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552561
Supporting Variants
Samples
Known GenesCSNK1G1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751308
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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