A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263016



Internal ID20472234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38743305..38743377hg38UCSC Ensembl
chr19:39233945..39234017hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747230
Supporting Variants
Samples
Known GenesCAPN12
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263016
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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