A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623211



Internal ID6663379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50582984..50584644hg38UCSC Ensembl
Innerchr10:50582985..50584644hg38UCSC Ensembl
Outerchr10:50582984..50584645hg38UCSC Ensembl
chr10:52342744..52344404hg19UCSC Ensembl
Innerchr10:52342745..52344404hg19UCSC Ensembl
Outerchr10:52342744..52344405hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg381661
hg191661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13803079, essv13803084, essv13803081, essv13803085, essv13803087, essv13803086, essv13803083, essv13803082, essv13803080
SamplesHG04131, HG04202, HG03642, HG03836, HG04219, HG03953, HG04198, HG03743, HG03702
Known GenesSGMS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623211
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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