A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13970335



Internal ID3972151
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624896
Supporting Variants
SamplesHG00698
Known GenesMKI67
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13970335
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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