A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10980901



Internal ID982717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36375559..36404508hg38UCSC Ensembl
chr3:36417051..36446000hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3828950
hg1928950
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595861
Supporting Variants
SamplesHG04155
Known GenesSTAC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10980901
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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