A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617443



Internal ID7004328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64170665..64198473hg38UCSC Ensembl
Innerchr8:64170665..64198473hg38UCSC Ensembl
Outerchr8:64170165..64198973hg38UCSC Ensembl
chr8:65083222..65111030hg19UCSC Ensembl
Innerchr8:65083222..65111030hg19UCSC Ensembl
Outerchr8:65082722..65111530hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3827809
hg1927809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13213192
SamplesNA20339
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617443
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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