A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7837018



Internal ID14691604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95679127..95679128hg38UCSC Ensembl
Innerchr13:95679084..95679171hg38UCSC Ensembl
Outerchr13:95679083..95679172hg38UCSC Ensembl
chr13:96331381..96331382hg19UCSC Ensembl
Innerchr13:96331338..96331425hg19UCSC Ensembl
Outerchr13:96331337..96331426hg19UCSC Ensembl
chr13:95129382..95129383hg18UCSC Ensembl
Innerchr13:95129426..95129339hg18UCSC Ensembl
Outerchr13:95129338..95129427hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381673
hg191673
hg181673
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3307890
Supporting Variants
SamplesNA19239
Known GenesDNAJC3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7837018
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