A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622657



Internal ID6662826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24858742..24864356hg38UCSC Ensembl
Innerchr10:24858774..24864324hg38UCSC Ensembl
Outerchr10:24858710..24864388hg38UCSC Ensembl
chr10:25147671..25153285hg19UCSC Ensembl
Innerchr10:25147703..25153253hg19UCSC Ensembl
Outerchr10:25147639..25153317hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg385615
hg195615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13721447, essv13721446
SamplesHG03556, HG02108
Known GenesPRTFDC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622657
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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