A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13764215



Internal ID1388202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42881030..42895811hg38UCSC Ensembl
Innerchr10:42881037..42895804hg38UCSC Ensembl
Outerchr10:42881023..42895818hg38UCSC Ensembl
chr10:43376478..43391259hg19UCSC Ensembl
Innerchr10:43376485..43391252hg19UCSC Ensembl
Outerchr10:43376471..43391266hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3814782
hg1914782
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623031
Supporting Variants
SamplesHG01256
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13764215
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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