A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9760390



Internal ID18734636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:27092983..27093611hg38UCSC Ensembl
Outerchr3:27092875..27093742hg38UCSC Ensembl
Innerchr3:27134474..27135102hg19UCSC Ensembl
Outerchr3:27134366..27135233hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38868
hg19868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3561643
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9760390
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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