A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624841



Internal ID7011691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125703366..125704975hg38UCSC Ensembl
Innerchr10:125703366..125704975hg38UCSC Ensembl
Outerchr10:125703139..125705161hg38UCSC Ensembl
chr10:127391935..127393544hg19UCSC Ensembl
Innerchr10:127391935..127393544hg19UCSC Ensembl
Outerchr10:127391708..127393730hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381610
hg191610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13964287
SamplesHG03096
Known GenesLOC283038
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624841
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