A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622587



Internal ID7009445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21768549..21786918hg38UCSC Ensembl
Innerchr10:21768553..21786914hg38UCSC Ensembl
Outerchr10:21768545..21786922hg38UCSC Ensembl
chr10:22057478..22075847hg19UCSC Ensembl
Innerchr10:22057482..22075843hg19UCSC Ensembl
Outerchr10:22057474..22075851hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3818370
hg1918370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13715475
SamplesHG00132
Known GenesDNAJC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622587
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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