A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7836966



Internal ID15038164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10422715..10422716hg38UCSC Ensembl
Innerchr5:10422684..10422747hg38UCSC Ensembl
Outerchr5:10422683..10422748hg38UCSC Ensembl
chr5:10422827..10422828hg19UCSC Ensembl
Innerchr5:10422796..10422859hg19UCSC Ensembl
Outerchr5:10422795..10422860hg19UCSC Ensembl
chr5:10475827..10475828hg18UCSC Ensembl
Innerchr5:10475859..10475796hg18UCSC Ensembl
Outerchr5:10475795..10475860hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38176
hg19176
hg18176
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3309619
Supporting Variants
SamplesNA19239
Known GenesMARCH6
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7836966
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