A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963919



Internal ID22738855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75994045..75994045hg38UCSC Ensembl
chr4:76915198..76915198hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963919
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer