A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13749838



Internal ID6380319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31965662..31984025hg38UCSC Ensembl
Innerchr10:31965673..31984015hg38UCSC Ensembl
Outerchr10:31965652..31984036hg38UCSC Ensembl
chr10:32254590..32272953hg19UCSC Ensembl
Innerchr10:32254601..32272943hg19UCSC Ensembl
Outerchr10:32254580..32272964hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3818364
hg1918364
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622819
Supporting Variants
SamplesNA20320
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13749838
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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