A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623496



Internal ID7010352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62407879..62413714hg38UCSC Ensembl
Innerchr10:62407879..62413714hg38UCSC Ensembl
Outerchr10:62407519..62413974hg38UCSC Ensembl
chr10:64167638..64173473hg19UCSC Ensembl
Innerchr10:64167638..64173473hg19UCSC Ensembl
Outerchr10:64167278..64173733hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg385836
hg195836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13833483, essv13833484, essv13833485, essv13833486, essv13833488, essv13833482, essv13833487, essv13833490, essv13833489, essv13833480, essv13833481
SamplesHG03558, HG02804, NA19307, HG03246, NA19024, NA19471, HG02479, HG02429, HG02884, NA19835, HG02855
Known GenesZNF365
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623496
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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