A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11049092



Internal ID822869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77776490..77796316hg38UCSC Ensembl
Innerchr3:77776640..77796166hg38UCSC Ensembl
Outerchr3:77776340..77796466hg38UCSC Ensembl
chr3:77825641..77845467hg19UCSC Ensembl
Innerchr3:77825791..77845317hg19UCSC Ensembl
Outerchr3:77825491..77845617hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3819827
hg1919827
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596667
Supporting Variants
SamplesHG00409
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11049092
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