A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640940



Internal ID6681025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60966399..60968234hg38UCSC Ensembl
Innerchr17:60966404..60968229hg38UCSC Ensembl
Outerchr17:60966394..60968239hg38UCSC Ensembl
chr17:59043760..59045595hg19UCSC Ensembl
Innerchr17:59043765..59045590hg19UCSC Ensembl
Outerchr17:59043755..59045600hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg381836
hg191836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15716444
SamplesNA18986
Known GenesBCAS3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640940
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