A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622416



Internal ID6662586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14123961..14126827hg38UCSC Ensembl
Innerchr10:14124011..14126777hg38UCSC Ensembl
Outerchr10:14123854..14126934hg38UCSC Ensembl
chr10:14165960..14168826hg19UCSC Ensembl
Innerchr10:14166010..14168776hg19UCSC Ensembl
Outerchr10:14165853..14168933hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382867
hg192867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13700551, essv13700550, essv13700549
SamplesNA18953, HG02521, NA18983
Known GenesFRMD4A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622416
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer