A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450877



Internal ID22508750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17690025..17706621hg38UCSC Ensembl
chr12:17842959..17859555hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3816597
hg1916597
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858324
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450877
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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