A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623482



Internal ID7010338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61539679..61544859hg38UCSC Ensembl
chr10:63299437..63304617hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg385181
hg195181
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13833447
SamplesHG00583
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623482
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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