A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190736



Internal ID20757776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25377086..25380611hg38UCSC Ensembl
chr16:25388407..25391932hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg383526
hg193526
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513031
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190736
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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