A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201031



Internal ID20768071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17336224..17352111hg38UCSC Ensembl
chr1:17662719..17678606hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3815888
hg1915888
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324500
Supporting Variants
Samples
Known GenesPADI4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201031
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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