A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623506



Internal ID7010362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63339353..63340812hg38UCSC Ensembl
Innerchr10:63339357..63340809hg38UCSC Ensembl
Outerchr10:63339350..63340816hg38UCSC Ensembl
chr10:65099113..65100572hg19UCSC Ensembl
Innerchr10:65099117..65100569hg19UCSC Ensembl
Outerchr10:65099110..65100576hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381460
hg191460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13835148, essv13835153, essv13835147, essv13835152, essv13835149, essv13835150, essv13835151, essv13835154
SamplesNA18745, NA18959, NA18748, NA19084, NA18945, NA19072, HG00631, HG00728
Known GenesJMJD1C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623506
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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