A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189629



Internal ID20756669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12293696..12306452hg38UCSC Ensembl
chr16:12387553..12400309hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3812757
hg1912757
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509548
Supporting Variants
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189629
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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