A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179220



Internal ID20746260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16613001..16622100hg38UCSC Ensembl
chr17:16516315..16525414hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg389100
hg199100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496003
Supporting Variants
Samples
Known GenesZNF624
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179220
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00031


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