A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3424204



Internal ID14924475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9627357..9627403hg38UCSC Ensembl
Innerchr5:9627373..9627385hg38UCSC Ensembl
Outerchr5:9627327..9627431hg38UCSC Ensembl
chr5:9627469..9627515hg19UCSC Ensembl
Innerchr5:9627485..9627497hg19UCSC Ensembl
Outerchr5:9627439..9627543hg19UCSC Ensembl
chr5:9680469..9680515hg18UCSC Ensembl
Innerchr5:9680497..9680485hg18UCSC Ensembl
Outerchr5:9680439..9680543hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38276
hg19276
hg18276
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8923307, essv8923308, essv8923309
SamplesNA18853, NA19257, NA19108
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3424204
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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