A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363341



Internal ID22589010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:4891875..4892047hg38UCSC Ensembl
chr12:5001041..5001213hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909637
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363341
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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