A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596793



Internal ID6984107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:83493310..83621137hg38UCSC Ensembl
Innerchr3:83493310..83621137hg38UCSC Ensembl
Outerchr3:83492810..83621637hg38UCSC Ensembl
chr3:83542461..83670288hg19UCSC Ensembl
Innerchr3:83542461..83670288hg19UCSC Ensembl
Outerchr3:83541961..83670788hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38127828
hg19127828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11058719
SamplesHG02052
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596793
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