A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595915



Internal ID6983233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38816484..38821828hg38UCSC Ensembl
Innerchr3:38816484..38821828hg38UCSC Ensembl
Outerchr3:38816386..38821936hg38UCSC Ensembl
chr3:38857975..38863319hg19UCSC Ensembl
Innerchr3:38857975..38863319hg19UCSC Ensembl
Outerchr3:38857877..38863427hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg385345
hg195345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10987419
SamplesHG03120
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595915
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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