A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7841948



Internal ID15083583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38919908..38919909hg38UCSC Ensembl
Innerchr13:38919887..38919930hg38UCSC Ensembl
Outerchr13:38919886..38919931hg38UCSC Ensembl
chr13:39494045..39494046hg19UCSC Ensembl
Innerchr13:39494024..39494067hg19UCSC Ensembl
Outerchr13:39494023..39494068hg19UCSC Ensembl
chr13:38392045..38392046hg18UCSC Ensembl
Innerchr13:38392067..38392024hg18UCSC Ensembl
Outerchr13:38392023..38392068hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38260
hg19260
hg18260
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3309010
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7841948
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