A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9760204



Internal ID18387764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:10355849..10356122hg38UCSC Ensembl
Outerchr3:10355774..10356197hg38UCSC Ensembl
Innerchr3:10397533..10397806hg19UCSC Ensembl
Outerchr3:10397458..10397881hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38424
hg19424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3561457
Supporting Variants
Samples
Known GenesATP2B2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9760204
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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