A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623041



Internal ID7009898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43349372..43357838hg38UCSC Ensembl
Innerchr10:43349872..43357338hg38UCSC Ensembl
Outerchr10:43348372..43358838hg38UCSC Ensembl
chr10:43844820..43853286hg19UCSC Ensembl
Innerchr10:43845320..43852786hg19UCSC Ensembl
Outerchr10:43843820..43854286hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg388467
hg198467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13764239
SamplesNA20510
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623041
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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