A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9750942



Internal ID18725188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23747040..23750353hg38UCSC Ensembl
Outerchr15:23746854..23750877hg38UCSC Ensembl
Innerchr15:23992187..23995500hg19UCSC Ensembl
Outerchr15:23992001..23996024hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg384024
hg194024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552195
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9750942
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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