A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622607



Internal ID7009465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23024008..23024733hg38UCSC Ensembl
Innerchr10:23024008..23024733hg38UCSC Ensembl
Outerchr10:23023751..23024984hg38UCSC Ensembl
chr10:23312937..23313662hg19UCSC Ensembl
Innerchr10:23312937..23313662hg19UCSC Ensembl
Outerchr10:23312680..23313913hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38726
hg19726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13716104
SamplesNA18636
Known GenesARMC3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622607
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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