A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624897



Internal ID7011747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128148393..128151932hg38UCSC Ensembl
Innerchr10:128148393..128151932hg38UCSC Ensembl
Outerchr10:128148175..128152146hg38UCSC Ensembl
chr10:129946657..129950196hg19UCSC Ensembl
Innerchr10:129946657..129950196hg19UCSC Ensembl
Outerchr10:129946439..129950410hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg383540
hg193540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13970337
SamplesHG01190
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624897
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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