A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623856



Internal ID6664023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75784550..75942028hg38UCSC Ensembl
Innerchr10:75784700..75941878hg38UCSC Ensembl
Outerchr10:75784400..75942178hg38UCSC Ensembl
chr10:77544308..77701786hg19UCSC Ensembl
Innerchr10:77544458..77701636hg19UCSC Ensembl
Outerchr10:77544158..77701936hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38157479
hg19157479
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13864452, essv13864453
SamplesNA19917, NA12872
Known GenesC10orf11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623856
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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