A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5570810



Internal ID21519180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94953923..94953992hg38UCSC Ensembl
chr5:94289627..94289696hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151667
SamplesHG00512
Known GenesMCTP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5570810
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