A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622282



Internal ID7009141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8086608..8087809hg38UCSC Ensembl
Innerchr10:8086621..8087796hg38UCSC Ensembl
Outerchr10:8086595..8087822hg38UCSC Ensembl
chr10:8128571..8129772hg19UCSC Ensembl
Innerchr10:8128584..8129759hg19UCSC Ensembl
Outerchr10:8128558..8129785hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13690313
SamplesHG02150
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622282
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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