A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617401



Internal ID7004286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61937510..61948520hg38UCSC Ensembl
Innerchr8:61937510..61948520hg38UCSC Ensembl
Outerchr8:61937010..61949020hg38UCSC Ensembl
chr8:62850069..62861079hg19UCSC Ensembl
Innerchr8:62850069..62861079hg19UCSC Ensembl
Outerchr8:62849569..62861579hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3811011
hg1911011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13211452
SamplesNA21144
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617401
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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