A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623192



Internal ID7010049
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13802451, essv13802450
SamplesHG03212, HG03470
Known GenesFLJ31813
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623192
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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