A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995908



Internal ID20562948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104369047..104370754hg38UCSC Ensembl
chr12:104762825..104764532hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381708
hg191708
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462191
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995908
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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