A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15655838



Internal ID2277959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28265275..28266019hg38UCSC Ensembl
Innerchr17:28265325..28265969hg38UCSC Ensembl
Outerchr17:28265141..28266153hg38UCSC Ensembl
chr17:26592301..26593045hg19UCSC Ensembl
Innerchr17:26592351..26592995hg19UCSC Ensembl
Outerchr17:26592167..26593179hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38745
hg19745
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640307
Supporting Variants
SamplesHG02032
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15655838
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