A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859322



Internal ID22634257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66996638..67002051hg38UCSC Ensembl
chr13:67570770..67576183hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg385414
hg195414
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458626
Samples
Known GenesPCDH9, PCDH9-AS4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859322
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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