A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595385



Internal ID6982703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15531930..15532518hg38UCSC Ensembl
Innerchr3:15531932..15532516hg38UCSC Ensembl
Outerchr3:15531928..15532520hg38UCSC Ensembl
chr3:15573437..15574025hg19UCSC Ensembl
Innerchr3:15573439..15574023hg19UCSC Ensembl
Outerchr3:15573435..15574027hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38589
hg19589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10933258
SamplesHG00443
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595385
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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