A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13764987



Internal ID454209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44261796..44265806hg38UCSC Ensembl
Innerchr10:44261796..44265806hg38UCSC Ensembl
Outerchr10:44261624..44266031hg38UCSC Ensembl
chr10:44757244..44761254hg19UCSC Ensembl
Innerchr10:44757244..44761254hg19UCSC Ensembl
Outerchr10:44757072..44761479hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg384011
hg194011
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623060
Supporting Variants
SamplesHG00143
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13764987
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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