A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618774



Internal ID7005656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127483634..127521565hg38UCSC Ensembl
Innerchr8:127483634..127521565hg38UCSC Ensembl
Outerchr8:127483134..127522065hg38UCSC Ensembl
chr8:128495879..128533810hg19UCSC Ensembl
Innerchr8:128495879..128533810hg19UCSC Ensembl
Outerchr8:128495379..128534310hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3837932
hg1937932
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1418e214
Supporting Variantsessv13322217
SamplesHG03488
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618774
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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