A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622517



Internal ID7009376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18771751..18795196hg38UCSC Ensembl
chr10:19060680..19084125hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3823446
hg1923446
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13710256
SamplesNA19378
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622517
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