A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595171



Internal ID6982489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:6686494..6687180hg38UCSC Ensembl
Innerchr3:6686537..6687138hg38UCSC Ensembl
Outerchr3:6686452..6687223hg38UCSC Ensembl
chr3:6728181..6728867hg19UCSC Ensembl
Innerchr3:6728224..6728825hg19UCSC Ensembl
Outerchr3:6728139..6728910hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38687
hg19687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10911228
SamplesHG01269
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595171
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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