A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17448612



Internal ID22506482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1850724..1850724hg38UCSC Ensembl
chr9:1850724..1850724hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5960683
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17448612
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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