A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17414854



Internal ID22472724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38949273..38949273hg38UCSC Ensembl
chr4:38950894..38950894hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5957016
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17414854
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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