A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618352



Internal ID7005234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:108264567..108272487hg38UCSC Ensembl
Innerchr8:108264567..108272487hg38UCSC Ensembl
Outerchr8:108264380..108272676hg38UCSC Ensembl
chr8:109276796..109284716hg19UCSC Ensembl
Innerchr8:109276796..109284716hg19UCSC Ensembl
Outerchr8:109276609..109284905hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg387921
hg197921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13281024, essv13281026, essv13281025
SamplesHG03436, HG00731, HG00320
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618352
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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