A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469564



Internal ID22527454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:91177782..91180018hg38UCSC Ensembl
chr12:91571559..91573795hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg382237
hg192237
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851711
Supporting Variants
Samples
Known GenesDCN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469564
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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