A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199884



Internal ID20766924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20647162..20652009hg38UCSC Ensembl
chr1:20973655..20978502hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg384848
hg194848
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327187
Supporting Variants
Samples
Known GenesDDOST, PINK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199884
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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