A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13715486



Internal ID6596020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22138873..22146004hg38UCSC Ensembl
Innerchr10:22138923..22145954hg38UCSC Ensembl
Outerchr10:22138800..22146077hg38UCSC Ensembl
chr10:22427802..22434933hg19UCSC Ensembl
Innerchr10:22427852..22434883hg19UCSC Ensembl
Outerchr10:22427729..22435006hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg387132
hg197132
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622591
Supporting Variants
SamplesNA20770
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13715486
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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