A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624890



Internal ID7011740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127755197..127791540hg38UCSC Ensembl
Innerchr10:127755197..127791540hg38UCSC Ensembl
Outerchr10:127754697..127792040hg38UCSC Ensembl
chr10:129553461..129589804hg19UCSC Ensembl
Innerchr10:129553461..129589804hg19UCSC Ensembl
Outerchr10:129552961..129590304hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3836344
hg1936344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13970259
SamplesHG02805
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624890
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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