A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029995



Internal ID20597035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50105309..50115900hg38UCSC Ensembl
chr16:50139220..50149811hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3810592
hg1910592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509297
Supporting Variants
Samples
Known GenesHEATR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029995
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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