A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13751429



Internal ID2992852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33908123..33914481hg38UCSC Ensembl
Innerchr10:33908124..33914481hg38UCSC Ensembl
Outerchr10:33908123..33914482hg38UCSC Ensembl
chr10:34197051..34203409hg19UCSC Ensembl
Innerchr10:34197052..34203409hg19UCSC Ensembl
Outerchr10:34197051..34203410hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg386359
hg196359
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622860
Supporting Variants
SamplesHG02643
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13751429
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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