A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618920



Internal ID7005802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:135257114..135268915hg38UCSC Ensembl
Innerchr8:135257114..135268915hg38UCSC Ensembl
Outerchr8:135256981..135269086hg38UCSC Ensembl
chr8:136269357..136281158hg19UCSC Ensembl
Innerchr8:136269357..136281158hg19UCSC Ensembl
Outerchr8:136269224..136281329hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3811802
hg1911802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13339034
SamplesHG03738
Known GenesLOC286094
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618920
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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