A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467907



Internal ID22525796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:5501074..5504673hg38UCSC Ensembl
chr12:5610240..5613839hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861978
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467907
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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