A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367252



Internal ID22592921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17022173..17027217hg38UCSC Ensembl
chr12:17175107..17180151hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg385045
hg195045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924657
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367252
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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