A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640968



Internal ID7027742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62351672..62354303hg38UCSC Ensembl
Innerchr17:62351693..62354283hg38UCSC Ensembl
Outerchr17:62351652..62354324hg38UCSC Ensembl
chr17:60429033..60431664hg19UCSC Ensembl
Innerchr17:60429054..60431644hg19UCSC Ensembl
Outerchr17:60429013..60431685hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg382632
hg192632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15717394, essv15717397, essv15717395, essv15717396
SamplesHG03755, NA19072, HG03955, HG03698
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640968
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