A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640288



Internal ID7027063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27221337..27247355hg38UCSC Ensembl
Innerchr17:27221344..27247348hg38UCSC Ensembl
Outerchr17:27221330..27247362hg38UCSC Ensembl
chr17:25548363..25574381hg19UCSC Ensembl
Innerchr17:25548370..25574374hg19UCSC Ensembl
Outerchr17:25548356..25574388hg19UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3826019
hg1926019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15653069
SamplesHG03229
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640288
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