A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3544261



Internal ID18745337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:134991450..134996757hg38UCSC Ensembl
Outerchr8:134990258..134998006hg38UCSC Ensembl
Innerchr8:136003693..136009000hg19UCSC Ensembl
Outerchr8:136002501..136010249hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg387749
hg197749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9743008
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3544261
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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