A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616155



Internal ID6656352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8898539..8904125hg38UCSC Ensembl
Innerchr8:8899039..8903625hg38UCSC Ensembl
Outerchr8:8897539..8905125hg38UCSC Ensembl
chr8:8756049..8761635hg19UCSC Ensembl
Innerchr8:8756549..8761135hg19UCSC Ensembl
Outerchr8:8755049..8762635hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg385587
hg195587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13093739
SamplesNA18978
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616155
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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