A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17405289



Internal ID22463159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9569689..9570000hg38UCSC Ensembl
chr20:9550336..9550647hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931873
Supporting Variants
Samples
Known GenesPAK7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17405289
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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