A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028663



Internal ID20595703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12013788..12019257hg38UCSC Ensembl
chr16:12107645..12113114hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg385470
hg195470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514308
Supporting Variants
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028663
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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