A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18002695



Internal ID20569735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:68153888..68154458hg38UCSC Ensembl
chr12:68547668..68548238hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470283
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18002695
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00072


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