A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475058



Internal ID22532953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50412973..50417420hg38UCSC Ensembl
chr17:48490334..48494781hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg384448
hg194448
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869958
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475058
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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