A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624094



Internal ID7010950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86584251..86586606hg38UCSC Ensembl
Innerchr10:86584271..86586587hg38UCSC Ensembl
Outerchr10:86584232..86586626hg38UCSC Ensembl
chr10:88344008..88346363hg19UCSC Ensembl
Innerchr10:88344028..88346344hg19UCSC Ensembl
Outerchr10:88343989..88346383hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg382356
hg192356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13883965
SamplesHG03548
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624094
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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