A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13935567



Internal ID5758528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111082548..111085586hg38UCSC Ensembl
Innerchr10:111082548..111085586hg38UCSC Ensembl
Outerchr10:111082493..111085628hg38UCSC Ensembl
chr10:112842306..112845344hg19UCSC Ensembl
Innerchr10:112842306..112845344hg19UCSC Ensembl
Outerchr10:112842251..112845386hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg383039
hg193039
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624547
Supporting Variants
SamplesNA19130
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13935567
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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