A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437492



Internal ID22495362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117453804..117453804hg38UCSC Ensembl
chr9:120216082..120216082hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961829
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437492
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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