A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624343



Internal ID7011199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98920932..98926085hg38UCSC Ensembl
Innerchr10:98920938..98926080hg38UCSC Ensembl
Outerchr10:98920927..98926091hg38UCSC Ensembl
chr10:100680689..100685842hg19UCSC Ensembl
Innerchr10:100680695..100685837hg19UCSC Ensembl
Outerchr10:100680684..100685848hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg385154
hg195154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13911425
SamplesHG03746
Known GenesHPSE2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624343
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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