A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466002



Internal ID22523893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55564746..55574801hg38UCSC Ensembl
chr12:55958530..55968585hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg3810056
hg1910056
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851811
Supporting Variants
Samples
Known GenesOR2AP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466002
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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