A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139252



Internal ID20706292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162090797..162375645hg38UCSC Ensembl
chr6:162511829..162796677hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38284849
hg19284849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610079
Supporting Variants
Samples
Known GenesPARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139252
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00038


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