A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179951



Internal ID20746991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41504823..41537119hg38UCSC Ensembl
chr17:39661075..39693371hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3832297
hg1932297
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514687
Supporting Variants
Samples
Known GenesKRT13, KRT15, KRT19, MIR6510
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179951
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00081


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