A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5957232



Internal ID22732360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88230888..88230888hg38UCSC Ensembl
chr9:90845803..90845803hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5957232
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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