A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13933202



Internal ID4962199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:109165063..109287174hg38UCSC Ensembl
Innerchr10:109165073..109287165hg38UCSC Ensembl
Outerchr10:109165054..109287184hg38UCSC Ensembl
chr10:110924821..111046932hg19UCSC Ensembl
Innerchr10:110924831..111046923hg19UCSC Ensembl
Outerchr10:110924812..111046942hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38122112
hg19122112
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624516
Supporting Variants
SamplesNA12842
Known GenesRNU6-53P
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13933202
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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