A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8740966



Internal ID15085396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32986409..32986423hg38UCSC Ensembl
Innerchr1:32986408..32986424hg38UCSC Ensembl
Outerchr1:32986359..32986473hg38UCSC Ensembl
chr1:33452010..33452024hg19UCSC Ensembl
Innerchr1:33452009..33452025hg19UCSC Ensembl
Outerchr1:33451960..33452074hg19UCSC Ensembl
chr1:33224597..33224611hg18UCSC Ensembl
Innerchr1:33224612..33224596hg18UCSC Ensembl
Outerchr1:33224547..33224661hg18UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38456
hg19456
hg18456
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3348537
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8740966
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