A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624525



Internal ID7011378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:109699681..109700331hg38UCSC Ensembl
Innerchr10:109699691..109700322hg38UCSC Ensembl
Outerchr10:109699672..109700341hg38UCSC Ensembl
chr10:111459439..111460089hg19UCSC Ensembl
Innerchr10:111459449..111460080hg19UCSC Ensembl
Outerchr10:111459430..111460099hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13933217
SamplesHG01111
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624525
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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