A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375746



Internal ID22601415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:52813430..52813430hg38UCSC Ensembl
chr17:50890790..50890790hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977433
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375746
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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