A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622652



Internal ID7009510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24759817..24770221hg38UCSC Ensembl
chr10:25048746..25059150hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3810405
hg1910405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13721426, essv13721427, essv13721428, essv13721429
SamplesHG03018, HG02491, HG03663, HG03491
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622652
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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