A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623153



Internal ID6663321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48355632..48366278hg38UCSC Ensembl
Innerchr10:48355632..48366278hg38UCSC Ensembl
Outerchr10:48355132..48366778hg38UCSC Ensembl
chr10:49563675..49574321hg19UCSC Ensembl
Innerchr10:49563675..49574321hg19UCSC Ensembl
Outerchr10:49563175..49574821hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3810647
hg1910647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13796089
SamplesHG03018
Known GenesMAPK8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623153
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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