A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10947416



Internal ID4591766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21528979..21540449hg38UCSC Ensembl
chr3:21570471..21581941hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3811471
hg1911471
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595513
Supporting Variants
SamplesHG04100
Known GenesZNF385D
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10947416
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