A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623504



Internal ID7010360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63270252..63271651hg38UCSC Ensembl
Innerchr10:63270252..63271651hg38UCSC Ensembl
Outerchr10:63269937..63271900hg38UCSC Ensembl
chr10:65030012..65031411hg19UCSC Ensembl
Innerchr10:65030012..65031411hg19UCSC Ensembl
Outerchr10:65029697..65031660hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13835137, essv13835139, essv13835138, essv13835132, essv13835134, essv13835136, essv13835140, essv13835133, essv13835135
SamplesHG03378, NA19456, NA19921, NA19401, HG03461, NA19072, HG02462, NA19711, NA19429
Known GenesJMJD1C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623504
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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