A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464992



Internal ID22522880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:68999663..69007590hg38UCSC Ensembl
chr12:69393443..69401370hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg387928
hg197928
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854732
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464992
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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