A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624031



Internal ID7010887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84359635..84360266hg38UCSC Ensembl
Innerchr10:84359666..84360236hg38UCSC Ensembl
Outerchr10:84359605..84360297hg38UCSC Ensembl
chr10:86119391..86120022hg19UCSC Ensembl
Innerchr10:86119422..86119992hg19UCSC Ensembl
Outerchr10:86119361..86120053hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38632
hg19632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13881986
SamplesHG01958
Known GenesCCSER2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624031
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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