A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624680



Internal ID7011530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117719520..117721391hg38UCSC Ensembl
Innerchr10:117719523..117721388hg38UCSC Ensembl
Outerchr10:117719517..117721394hg38UCSC Ensembl
chr10:119479031..119480902hg19UCSC Ensembl
Innerchr10:119479034..119480899hg19UCSC Ensembl
Outerchr10:119479028..119480905hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381872
hg191872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13946572
SamplesHG04212
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624680
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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