A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641138



Internal ID7027912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69904807..69905318hg38UCSC Ensembl
Innerchr17:69904809..69905317hg38UCSC Ensembl
Outerchr17:69904806..69905320hg38UCSC Ensembl
chr17:67900948..67901459hg19UCSC Ensembl
Innerchr17:67900950..67901458hg19UCSC Ensembl
Outerchr17:67900947..67901461hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15731868, essv15731869, essv15731867, essv15731866
SamplesHG02922, HG02943, HG00479, HG03271
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641138
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer