A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596014



Internal ID6983332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43445989..43455734hg38UCSC Ensembl
Innerchr3:43445989..43455734hg38UCSC Ensembl
Outerchr3:43445844..43455820hg38UCSC Ensembl
chr3:43487481..43497226hg19UCSC Ensembl
Innerchr3:43487481..43497226hg19UCSC Ensembl
Outerchr3:43487336..43497312hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg389746
hg199746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10993069
SamplesHG03874
Known GenesANO10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596014
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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