A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9760713



Internal ID18734959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:61430356..61431128hg38UCSC Ensembl
Outerchr3:61430269..61431138hg38UCSC Ensembl
Innerchr3:61416030..61416802hg19UCSC Ensembl
Outerchr3:61415943..61416812hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38870
hg19870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3561966
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9760713
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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