A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751389



Internal ID18725635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70729809..70735095hg38UCSC Ensembl
Outerchr15:70729461..70735256hg38UCSC Ensembl
Innerchr15:71022148..71027434hg19UCSC Ensembl
Outerchr15:71021800..71027595hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg385796
hg195796
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552642
Supporting Variants
Samples
Known GenesUACA
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751389
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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