A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997089



Internal ID20564129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:115298024..115300864hg38UCSC Ensembl
chr12:115735829..115738669hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg382841
hg192841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491515
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997089
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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