A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10967981



Internal ID969797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:29312866..29316700hg38UCSC Ensembl
chr3:29354357..29358191hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg383835
hg193835
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595710
Supporting Variants
SamplesHG00160
Known GenesRBMS3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10967981
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