A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18001101



Internal ID20568141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:49076578..49078847hg38UCSC Ensembl
chr12:49470361..49472630hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg382270
hg192270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461338
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18001101
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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