A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13102268



Internal ID3655708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11165175..11192217hg38UCSC Ensembl
Innerchr8:11165228..11192165hg38UCSC Ensembl
Outerchr8:11165123..11192270hg38UCSC Ensembl
chr8:11022685..11049726hg19UCSC Ensembl
Innerchr8:11022738..11049674hg19UCSC Ensembl
Outerchr8:11022633..11049779hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3827043
hg1927042
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3616238
Supporting Variants
SamplesHG03258
Known GenesXKR6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13102268
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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