A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452155



Internal ID22510027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:133235783..133240818hg38UCSC Ensembl
chr12:133812369..133817404hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg385036
hg195036
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849896
Supporting Variants
Samples
Known GenesANHX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452155
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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