A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598897



Internal ID6985945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181895538..181897261hg38UCSC Ensembl
Innerchr3:181895542..181897258hg38UCSC Ensembl
Outerchr3:181895535..181897265hg38UCSC Ensembl
chr3:181613326..181615049hg19UCSC Ensembl
Innerchr3:181613330..181615046hg19UCSC Ensembl
Outerchr3:181613323..181615053hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg381724
hg191724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11251219
SamplesHG02471
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598897
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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