A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624160



Internal ID7011016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89540041..89550309hg38UCSC Ensembl
Innerchr10:89540191..89550159hg38UCSC Ensembl
Outerchr10:89539891..89550459hg38UCSC Ensembl
chr10:91299798..91310066hg19UCSC Ensembl
Innerchr10:91299948..91309916hg19UCSC Ensembl
Outerchr10:91299648..91310216hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3810269
hg1910269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13890788
SamplesHG01807
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624160
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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