A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624196



Internal ID7011052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:90928801..90977033hg38UCSC Ensembl
Innerchr10:90928801..90977033hg38UCSC Ensembl
Outerchr10:90928301..90977533hg38UCSC Ensembl
chr10:92688558..92736790hg19UCSC Ensembl
Innerchr10:92688558..92736790hg19UCSC Ensembl
Outerchr10:92688058..92737290hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3848233
hg1948233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13894266
SamplesNA19351
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624196
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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