A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7838757



Internal ID15007484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42658507..42658508hg38UCSC Ensembl
Innerchr6:42658478..42658537hg38UCSC Ensembl
Outerchr6:42658477..42658538hg38UCSC Ensembl
chr6:42626245..42626246hg19UCSC Ensembl
Innerchr6:42626216..42626275hg19UCSC Ensembl
Outerchr6:42626215..42626276hg19UCSC Ensembl
chr6:42734223..42734224hg18UCSC Ensembl
Innerchr6:42734253..42734194hg18UCSC Ensembl
Outerchr6:42734193..42734254hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38277
hg19277
hg18277
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3308392
Supporting Variants
SamplesNA19238
Known GenesUBR2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7838757
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