A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954807



Internal ID22730035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:176450529..176450529hg38UCSC Ensembl
chr4:177371680..177371680hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414150
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954807
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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