A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17358184



Internal ID22583853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122150109..122165977hg38UCSC Ensembl
chr12:122634656..122650524hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3815869
hg1915869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928227
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17358184
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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