A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624555



Internal ID7011408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111239334..111254388hg38UCSC Ensembl
Innerchr10:111239484..111254238hg38UCSC Ensembl
Outerchr10:111239184..111254538hg38UCSC Ensembl
chr10:112999092..113014146hg19UCSC Ensembl
Innerchr10:112999242..113013996hg19UCSC Ensembl
Outerchr10:112998942..113014296hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3815055
hg1915055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv165e214
Supporting Variantsessv13935584
SamplesNA20897
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624555
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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