A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439881



Internal ID22497751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91510812..91510812hg38UCSC Ensembl
chr9:94273094..94273094hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961360
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439881
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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