A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17998075



Internal ID20565116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:16342010..16424542hg38UCSC Ensembl
chr12:16494944..16577476hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3882533
hg1982533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466024
Supporting Variants
Samples
Known GenesMGST1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17998075
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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