A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622518



Internal ID7009377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18771890..18980142hg38UCSC Ensembl
Innerchr10:18771892..18980140hg38UCSC Ensembl
Outerchr10:18771888..18980144hg38UCSC Ensembl
chr10:19060819..19269071hg19UCSC Ensembl
Innerchr10:19060821..19269069hg19UCSC Ensembl
Outerchr10:19060817..19269073hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38208253
hg19208253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv101e214
Supporting Variantsessv13710257, essv13710258
SamplesNA19378, NA19334
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622518
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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