A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624216



Internal ID6664383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91999594..92001198hg38UCSC Ensembl
Innerchr10:91999607..92001185hg38UCSC Ensembl
Outerchr10:91999581..92001211hg38UCSC Ensembl
chr10:93759351..93760955hg19UCSC Ensembl
Innerchr10:93759364..93760942hg19UCSC Ensembl
Outerchr10:93759338..93760968hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg381605
hg191605
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13896519
SamplesNA18647
Known GenesBTAF1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624216
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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