A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17478894



Internal ID22536796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67555277..67556476hg38UCSC Ensembl
chr17:65551393..65552592hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870032
Supporting Variants
Samples
Known GenesPITPNC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17478894
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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