A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182857



Internal ID20749897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:60520301..60528500hg38UCSC Ensembl
chr16:60554205..60562404hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg388200
hg198200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502717
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182857
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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