A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9754690



Internal ID18728936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6152305..6152517hg38UCSC Ensembl
Outerchr19:6152271..6152571hg38UCSC Ensembl
Innerchr19:6152316..6152528hg19UCSC Ensembl
Outerchr19:6152282..6152582hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3555943
Supporting Variants
Samples
Known GenesACSBG2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9754690
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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