A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17387792



Internal ID22445662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:48105324..48105324hg38UCSC Ensembl
chr17:46182686..46182686hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968636
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17387792
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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