A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184730



Internal ID20751770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88162338..88258948hg38UCSC Ensembl
chr16:88195944..88292554hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3896611
hg1996611
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496961
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184730
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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