A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459961



Internal ID22517847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:96078894..96081025hg38UCSC Ensembl
chr12:96472672..96474803hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg382132
hg192132
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852168
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459961
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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