A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640865



Internal ID7027639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57018533..57028532hg38UCSC Ensembl
Innerchr17:57018533..57028532hg38UCSC Ensembl
Outerchr17:57018033..57029032hg38UCSC Ensembl
chr17:55095894..55105893hg19UCSC Ensembl
Innerchr17:55095894..55105893hg19UCSC Ensembl
Outerchr17:55095394..55106393hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3810000
hg1910000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15707751
SamplesHG00708
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640865
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