A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585675



Internal ID21534223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69326016..69327170hg38UCSC Ensembl
chr10:71085772..71086926hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381155
hg191155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071148
SamplesHG03683
Known GenesHK1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585675
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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