A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436610



Internal ID22494480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121298621..121298621hg38UCSC Ensembl
chr9:124060899..124060899hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5957868
Supporting Variants
Samples
Known GenesGSN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436610
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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