A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623779



Internal ID6663946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71546654..71549779hg38UCSC Ensembl
Innerchr10:71546654..71549779hg38UCSC Ensembl
Outerchr10:71546428..71550052hg38UCSC Ensembl
chr10:73306411..73309536hg19UCSC Ensembl
Innerchr10:73306411..73309536hg19UCSC Ensembl
Outerchr10:73306185..73309809hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg383126
hg193126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13860898, essv13860899
SamplesHG03742, HG04189
Known GenesCDH23
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623779
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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