A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622078



Internal ID7008937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:530057..594362hg38UCSC Ensembl
Innerchr10:530068..594351hg38UCSC Ensembl
Outerchr10:530046..594373hg38UCSC Ensembl
chr10:575997..640302hg19UCSC Ensembl
Innerchr10:576008..640291hg19UCSC Ensembl
Outerchr10:575986..640313hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3864306
hg1964306
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13664291
SamplesHG04227
Known GenesDIP2C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622078
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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