A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622122



Internal ID7008981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:2185403..2214514hg38UCSC Ensembl
Innerchr10:2185903..2214014hg38UCSC Ensembl
Outerchr10:2184403..2215514hg38UCSC Ensembl
chr10:2227597..2256708hg19UCSC Ensembl
Innerchr10:2228097..2256208hg19UCSC Ensembl
Outerchr10:2226597..2257708hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3829112
hg1929112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13667729
SamplesHG02360
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622122
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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