A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462759



Internal ID22520644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122736885..122741609hg38UCSC Ensembl
chr12:123221432..123226156hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg384725
hg194725
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863840
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462759
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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