A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624896



Internal ID6665058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128105981..128107086hg38UCSC Ensembl
Innerchr10:128106031..128107036hg38UCSC Ensembl
Outerchr10:128105931..128107136hg38UCSC Ensembl
chr10:129904245..129905350hg19UCSC Ensembl
Innerchr10:129904295..129905300hg19UCSC Ensembl
Outerchr10:129904195..129905400hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg381106
hg191106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13970336, essv13970335
SamplesNA20866, HG00698
Known GenesMKI67
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624896
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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