A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13848631



Internal ID1100465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67784938..67795564hg38UCSC Ensembl
Innerchr10:67785088..67795414hg38UCSC Ensembl
Outerchr10:67784788..67795714hg38UCSC Ensembl
chr10:69544696..69555322hg19UCSC Ensembl
Innerchr10:69544846..69555172hg19UCSC Ensembl
Outerchr10:69544546..69555472hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3810627
hg1910627
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623694
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13848631
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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