A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352384



Internal ID22578053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151760903..151760903hg38UCSC Ensembl
chr1:151733379..151733379hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5959881
Supporting Variants
Samples
Known GenesMRPL9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352384
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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