A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3442695



Internal ID14942962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241590164..241591262hg38UCSC Ensembl
Innerchr2:241590262..241591164hg38UCSC Ensembl
Outerchr2:241589164..241592262hg38UCSC Ensembl
chr2:242529579..242530677hg19UCSC Ensembl
Innerchr2:242529677..242530579hg19UCSC Ensembl
Outerchr2:242528579..242531677hg19UCSC Ensembl
chr2:242178252..242179350hg18UCSC Ensembl
Innerchr2:242179252..242178350hg18UCSC Ensembl
Outerchr2:242177252..242180350hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg381099
hg191099
hg181099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2379e59
Supporting Variantsessv8693571
SamplesNA19238
Known GenesTHAP4
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3442695
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