A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13802451



Internal ID3833495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50018390..50065879hg38UCSC Ensembl
Innerchr10:50018390..50065879hg38UCSC Ensembl
Outerchr10:50017890..50066379hg38UCSC Ensembl
chr10:51778150..51825639hg19UCSC Ensembl
Innerchr10:51778150..51825639hg19UCSC Ensembl
Outerchr10:51777650..51826139hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3847490
hg1947490
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623192
Supporting Variants
SamplesHG03470
Known GenesFLJ31813
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13802451
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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