A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623830



Internal ID6663997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74548239..74550344hg38UCSC Ensembl
Innerchr10:74548239..74550344hg38UCSC Ensembl
Outerchr10:74548013..74550535hg38UCSC Ensembl
chr10:76307997..76310102hg19UCSC Ensembl
Innerchr10:76307997..76310102hg19UCSC Ensembl
Outerchr10:76307771..76310293hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg382106
hg192106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13863624
SamplesNA19332
Known GenesADK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623830
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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