A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614363



Internal ID21562668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195771334..195771334hg38UCSC Ensembl
chr3:195498205..195498205hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123977
SamplesHG03371
Known GenesMUC4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614363
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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