A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411926



Internal ID22469796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:23199306..23199306hg38UCSC Ensembl
chr4:23200929..23200929hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5963368
Supporting Variants
Samples
Known GenesMIR548AJ2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411926
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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