A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947951



Internal ID22723443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37014997..37014997hg38UCSC Ensembl
chr4:37016619..37016619hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419700
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947951
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