A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182667



Internal ID20749707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35570087..35574100hg38UCSC Ensembl
chr17:33897106..33901119hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg384014
hg194014
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511313
Supporting Variants
Samples
Known GenesSNORD7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182667
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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