A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464462



Internal ID22522349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50785437..50802125hg38UCSC Ensembl
chr12:51179220..51195908hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg3816689
hg1916689
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858530
Supporting Variants
Samples
Known GenesATF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464462
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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