A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7736892



Internal ID13111418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:82415046..82415047hg38UCSC Ensembl
Outerchr1:82414888..82415206hg38UCSC Ensembl
Innerchr1:82880729..82880730hg19UCSC Ensembl
Outerchr1:82880571..82880889hg19UCSC Ensembl
Innerchr1:82653318..82653317hg18UCSC Ensembl
Outerchr1:82653159..82653477hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38319
hg19319
hg18319
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3303003
Supporting Variants
SamplesNA10851
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7736892
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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