A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623503



Internal ID7010359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63088091..63092512hg38UCSC Ensembl
Innerchr10:63088241..63092362hg38UCSC Ensembl
Outerchr10:63087941..63092662hg38UCSC Ensembl
chr10:64847851..64852272hg19UCSC Ensembl
Innerchr10:64848001..64852122hg19UCSC Ensembl
Outerchr10:64847701..64852422hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg384422
hg194422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13835131
SamplesHG01504
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623503
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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