A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579320



Internal ID21527799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81295764..81295815hg38UCSC Ensembl
chr5:80591583..80591634hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144776
SamplesHG03486
Known GenesCKMT2-AS1, RNU5D-1, RNU5E-1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579320
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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