A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13935769



Internal ID4201735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112057322..112058655hg38UCSC Ensembl
Innerchr10:112057372..112058605hg38UCSC Ensembl
Outerchr10:112057272..112058705hg38UCSC Ensembl
chr10:113817080..113818413hg19UCSC Ensembl
Innerchr10:113817130..113818363hg19UCSC Ensembl
Outerchr10:113817030..113818463hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381334
hg191334
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624572
Supporting Variants
SamplesHG03786
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13935769
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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