A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623212



Internal ID7010069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50632619..50632920hg38UCSC Ensembl
Innerchr10:50632625..50632914hg38UCSC Ensembl
Outerchr10:50632613..50632926hg38UCSC Ensembl
chr10:52392379..52392680hg19UCSC Ensembl
Innerchr10:52392385..52392674hg19UCSC Ensembl
Outerchr10:52392373..52392686hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13803088
SamplesNA19681
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623212
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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