A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625852



Internal ID21574157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81432773..81432773hg38UCSC Ensembl
chr5:80728592..80728592hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17146896
SamplesNA19239
Known GenesRNU5D-1, RNU5E-1, SSBP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625852
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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