A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353934



Internal ID22579603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:42304030..42306290hg38UCSC Ensembl
chr12:42697832..42700092hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg382261
hg192261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5947058
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353934
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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