A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18000349



Internal ID20567389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3964199..3969583hg38UCSC Ensembl
chr12:4073365..4078749hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg385385
hg195385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469573
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18000349
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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