A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617590



Internal ID7004475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:71445757..71466342hg38UCSC Ensembl
Innerchr8:71445757..71466342hg38UCSC Ensembl
Outerchr8:71445257..71466842hg38UCSC Ensembl
chr8:72357992..72378577hg19UCSC Ensembl
Innerchr8:72357992..72378577hg19UCSC Ensembl
Outerchr8:72357492..72379077hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3820586
hg1920586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13222004
SamplesHG03163
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617590
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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