A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598277



Internal ID6985413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155417713..155422564hg38UCSC Ensembl
Innerchr3:155417713..155422564hg38UCSC Ensembl
Outerchr3:155417453..155422798hg38UCSC Ensembl
chr3:155135502..155140353hg19UCSC Ensembl
Innerchr3:155135502..155140353hg19UCSC Ensembl
Outerchr3:155135242..155140587hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg384852
hg194852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11191741
SamplesHG00613
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598277
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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