A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5630614



Internal ID21578919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:91443651..91443651hg38UCSC Ensembl
chr5:90739468..90739468hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg383821
hg193821
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141216
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5630614
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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