A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13866685



Internal ID680291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78691610..78697484hg38UCSC Ensembl
Innerchr10:78691617..78697478hg38UCSC Ensembl
Outerchr10:78691604..78697491hg38UCSC Ensembl
chr10:80451367..80457241hg19UCSC Ensembl
Innerchr10:80451374..80457235hg19UCSC Ensembl
Outerchr10:80451361..80457248hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg385875
hg195875
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623898
Supporting Variants
SamplesHG00319
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13866685
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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