A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597286



Internal ID6972220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106303777..106308464hg38UCSC Ensembl
Innerchr3:106303777..106308464hg38UCSC Ensembl
Outerchr3:106303277..106308964hg38UCSC Ensembl
chr3:106022624..106027311hg19UCSC Ensembl
Innerchr3:106022624..106027311hg19UCSC Ensembl
Outerchr3:106022124..106027811hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg384688
hg194688
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11093511
SamplesHG01948
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597286
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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