A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599074



Internal ID6986122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190361787..190370018hg38UCSC Ensembl
Innerchr3:190362287..190369518hg38UCSC Ensembl
Outerchr3:190360787..190371018hg38UCSC Ensembl
chr3:190079576..190087807hg19UCSC Ensembl
Innerchr3:190080076..190087307hg19UCSC Ensembl
Outerchr3:190078576..190088807hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg388232
hg198232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11269135
SamplesHG00622
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599074
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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