A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467875



Internal ID22525765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122731141..122736584hg38UCSC Ensembl
chr12:123215688..123221131hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg385444
hg195444
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864117
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467875
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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