A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996228



Internal ID20563268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10886157..10893997hg38UCSC Ensembl
chr12:11038756..11046596hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg387841
hg197841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461167
Supporting Variants
Samples
Known GenesPRH1-PRR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996228
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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