A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705607



Internal ID21377883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67214974..67216683hg38UCSC Ensembl
chr13:67789106..67790815hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg381710
hg191710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390714
Supporting Variants
Samples
Known GenesPCDH9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705607
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0143678


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