A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv66n172



Internal ID22814440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4815521..4816030hg38UCSC Ensembl
chr10:4857713..4858222hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38510
hg19510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4431339, nsv4431338
SamplesNB07, MDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv66n172
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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