A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17478937



Internal ID22536839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76320646..76326761hg38UCSC Ensembl
chr17:74316727..74322842hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg386116
hg196116
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5886640
Supporting Variants
Samples
Known GenesPRPSAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17478937
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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