A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15320973



Internal ID2076548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92650335..92655706hg38UCSC Ensembl
Innerchr15:92650346..92655696hg38UCSC Ensembl
Outerchr15:92650325..92655717hg38UCSC Ensembl
chr15:93193565..93198936hg19UCSC Ensembl
Innerchr15:93193576..93198926hg19UCSC Ensembl
Outerchr15:93193555..93198947hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg385372
hg195372
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637267
Supporting Variants
SamplesHG01886
Known GenesFAM174B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15320973
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