A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622819



Internal ID7009677
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv106e214
Supporting Variantsessv13749838, essv13749839, essv13749837
SamplesNA20321, NA20320, NA19456
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622819
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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