A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9760821



Internal ID18735067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:74716283..74716545hg38UCSC Ensembl
Outerchr3:74716221..74716613hg38UCSC Ensembl
Innerchr3:74765434..74765696hg19UCSC Ensembl
Outerchr3:74765372..74765764hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3562074
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9760821
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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