A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640129



Internal ID7026906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17362860..17370527hg38UCSC Ensembl
Innerchr17:17363010..17370377hg38UCSC Ensembl
Outerchr17:17362710..17370677hg38UCSC Ensembl
chr17:17266174..17273841hg19UCSC Ensembl
Innerchr17:17266324..17273691hg19UCSC Ensembl
Outerchr17:17266024..17273991hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg387668
hg197668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15635773
SamplesNA19474
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640129
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