A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622308



Internal ID7009167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9450663..9453933hg38UCSC Ensembl
chr10:9492626..9495896hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg383271
hg193271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13691672
SamplesHG01190
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622308
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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