A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956417



Internal ID22731608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:149995133..149995133hg38UCSC Ensembl
chr4:150916285..150916285hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429130
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956417
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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