A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623163



Internal ID6663331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49074727..49075126hg38UCSC Ensembl
Innerchr10:49074757..49075096hg38UCSC Ensembl
Outerchr10:49074697..49075156hg38UCSC Ensembl
chr10:50282772..50283171hg19UCSC Ensembl
Innerchr10:50282802..50283141hg19UCSC Ensembl
Outerchr10:50282742..50283201hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13796115
SamplesNA19681
Known GenesVSTM4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623163
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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