A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5957137



Internal ID22732277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73115528..73115528hg38UCSC Ensembl
chr9:75730444..75730444hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447348
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5957137
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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