A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355091



Internal ID22580760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41100845..41124018hg38UCSC Ensembl
chr12:41494647..41517820hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3823174
hg1923174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936892
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355091
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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