A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996163



Internal ID20563203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:107672645..107675399hg38UCSC Ensembl
chr12:108066422..108069176hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg382755
hg192755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466744
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996163
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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