A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954304



Internal ID22704245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13676462..13676462hg38UCSC Ensembl
chr4:13678086..13678086hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419931
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954304
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