A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179704



Internal ID20746744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27670578..27924229hg38UCSC Ensembl
chr16:27681899..27935550hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38253652
hg19253652
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508222
Supporting Variants
Samples
Known GenesGSG1L, KIAA0556
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179704
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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