A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597694



Internal ID6984832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127528764..127537337hg38UCSC Ensembl
Innerchr3:127528914..127537187hg38UCSC Ensembl
Outerchr3:127528614..127537487hg38UCSC Ensembl
chr3:127247607..127256180hg19UCSC Ensembl
Innerchr3:127247757..127256030hg19UCSC Ensembl
Outerchr3:127247457..127256330hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg388574
hg198574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11135120
SamplesNA19043
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597694
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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