A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474389



Internal ID22532283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45020068..45024736hg38UCSC Ensembl
chr17:43097436..43102104hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg384669
hg194669
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874536
Supporting Variants
Samples
Known GenesDCAKD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474389
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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