A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617432



Internal ID7004317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63715288..63728892hg38UCSC Ensembl
Innerchr8:63715313..63728868hg38UCSC Ensembl
Outerchr8:63715264..63728917hg38UCSC Ensembl
chr8:64627846..64641450hg19UCSC Ensembl
Innerchr8:64627871..64641426hg19UCSC Ensembl
Outerchr8:64627822..64641475hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3813605
hg1913605
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13213160
SamplesNA18634
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617432
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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