A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11199655



Internal ID1201472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160436567..160440887hg38UCSC Ensembl
Innerchr3:160436617..160440837hg38UCSC Ensembl
Outerchr3:160436517..160440937hg38UCSC Ensembl
chr3:160154355..160158675hg19UCSC Ensembl
Innerchr3:160154405..160158625hg19UCSC Ensembl
Outerchr3:160154305..160158725hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg384321
hg194321
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598384
Supporting Variants
SamplesHG00356
Known GenesTRIM59
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11199655
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