A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452125



Internal ID22509997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:57688096..57693204hg38UCSC Ensembl
chr13:58262230..58267338hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg385109
hg195109
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861706
Supporting Variants
Samples
Known GenesPCDH17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452125
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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