A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069238



Internal ID20636278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9569689..9570001hg38UCSC Ensembl
chr20:9550336..9550648hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516514
Supporting Variants
Samples
Known GenesPAK7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069238
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00905


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