A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13803088



Internal ID6147218
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623212
Supporting Variants
SamplesNA19681
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13803088
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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