A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622735



Internal ID6662904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27871054..27879782hg38UCSC Ensembl
Innerchr10:27871054..27879782hg38UCSC Ensembl
Outerchr10:27870937..27879903hg38UCSC Ensembl
chr10:28159983..28168711hg19UCSC Ensembl
Innerchr10:28159983..28168711hg19UCSC Ensembl
Outerchr10:28159866..28168832hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg388729
hg198729
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13737693, essv13737691, essv13737692
SamplesHG02725, HG04198, HG03849
Known GenesARMC4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622735
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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