A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623502



Internal ID7010358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63060898..63062476hg38UCSC Ensembl
Innerchr10:63060948..63062426hg38UCSC Ensembl
Outerchr10:63060818..63062556hg38UCSC Ensembl
chr10:64820658..64822236hg19UCSC Ensembl
Innerchr10:64820708..64822186hg19UCSC Ensembl
Outerchr10:64820578..64822316hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381579
hg191579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13835130
SamplesHG01927
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623502
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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