A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10961177



Internal ID6098949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27795955..27801998hg38UCSC Ensembl
Innerchr3:27795959..27801995hg38UCSC Ensembl
Outerchr3:27795952..27802002hg38UCSC Ensembl
chr3:27837446..27843489hg19UCSC Ensembl
Innerchr3:27837450..27843486hg19UCSC Ensembl
Outerchr3:27837443..27843493hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg386044
hg196044
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595677
Supporting Variants
SamplesNA19475
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10961177
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