A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18000113



Internal ID20567153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27891107..27898155hg38UCSC Ensembl
chr12:28044040..28051088hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg387049
hg197049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468366
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18000113
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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