A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597251



Internal ID6972185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104382742..105065366hg38UCSC Ensembl
Innerchr3:104383242..105064866hg38UCSC Ensembl
Outerchr3:104381742..105066366hg38UCSC Ensembl
chr3:104101586..104784210hg19UCSC Ensembl
Innerchr3:104102086..104783710hg19UCSC Ensembl
Outerchr3:104100586..104785210hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38682625
hg19682625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11092053
SamplesNA18966
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597251
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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