A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622519



Internal ID7009378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18805063..18979875hg38UCSC Ensembl
chr10:19093992..19268804hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38174813
hg19174813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv101e214
Supporting Variantsessv13710259
SamplesNA19378
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622519
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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