A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18030235



Internal ID20597275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56656266..56673082hg38UCSC Ensembl
chr16:56690178..56706994hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3816817
hg1916817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514739
Supporting Variants
Samples
Known GenesMT1F, MT1G, MT1H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18030235
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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