A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352199



Internal ID22577868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:90515437..90551577hg38UCSC Ensembl
chr12:90909214..90945354hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3836141
hg1936141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936896
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352199
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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