A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13764244



Internal ID3769741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43391117..43392506hg38UCSC Ensembl
Innerchr10:43391132..43392491hg38UCSC Ensembl
Outerchr10:43391102..43392521hg38UCSC Ensembl
chr10:43886565..43887954hg19UCSC Ensembl
Innerchr10:43886580..43887939hg19UCSC Ensembl
Outerchr10:43886550..43887969hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg381390
hg191390
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623043
Supporting Variants
SamplesHG03401
Known GenesHNRNPF
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13764244
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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