A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13883956



Internal ID3885772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86400588..86405651hg38UCSC Ensembl
Innerchr10:86400588..86405651hg38UCSC Ensembl
Outerchr10:86400088..86406151hg38UCSC Ensembl
chr10:88160345..88165408hg19UCSC Ensembl
Innerchr10:88160345..88165408hg19UCSC Ensembl
Outerchr10:88159845..88165908hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg385064
hg195064
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624090
Supporting Variants
SamplesHG01777
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13883956
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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