A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595442



Internal ID6982760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18924513..18933266hg38UCSC Ensembl
Innerchr3:18925013..18932766hg38UCSC Ensembl
Outerchr3:18923513..18934266hg38UCSC Ensembl
chr3:18966005..18974758hg19UCSC Ensembl
Innerchr3:18966505..18974258hg19UCSC Ensembl
Outerchr3:18965005..18975758hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg388754
hg198754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10940411
SamplesHG03237
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595442
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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