A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595483



Internal ID6982801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20491926..20587811hg38UCSC Ensembl
Innerchr3:20491976..20587761hg38UCSC Ensembl
Outerchr3:20491876..20587861hg38UCSC Ensembl
chr3:20533418..20629303hg19UCSC Ensembl
Innerchr3:20533468..20629253hg19UCSC Ensembl
Outerchr3:20533368..20629353hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3895886
hg1995886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10946124
SamplesHG01808
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595483
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer