A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597022



Internal ID6984336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94349771..94350925hg38UCSC Ensembl
Innerchr3:94349783..94350913hg38UCSC Ensembl
Outerchr3:94349759..94350937hg38UCSC Ensembl
chr3:94068615..94069769hg19UCSC Ensembl
Innerchr3:94068627..94069757hg19UCSC Ensembl
Outerchr3:94068603..94069781hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg381155
hg191155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11069819, essv11069818
SamplesHG00844, HG01846
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597022
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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