A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624682



Internal ID7011532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117938174..117939297hg38UCSC Ensembl
Innerchr10:117938177..117939295hg38UCSC Ensembl
Outerchr10:117938172..117939300hg38UCSC Ensembl
chr10:119697685..119698808hg19UCSC Ensembl
Innerchr10:119697688..119698806hg19UCSC Ensembl
Outerchr10:119697683..119698811hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381124
hg191124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13946574
SamplesHG02283
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624682
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