A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995686



Internal ID20562726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104130556..104132357hg38UCSC Ensembl
chr12:104524334..104526135hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381802
hg191802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460457
Supporting Variants
Samples
Known GenesNFYB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995686
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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