A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180139



Internal ID20747179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39998423..39998948hg38UCSC Ensembl
chr17:38154676..38155201hg19UCSC Ensembl
Cytoband17q21.1
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503362
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180139
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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