A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296272



Internal ID20505490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11424537..11424649hg38UCSC Ensembl
chr19:11535206..11535320hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38113
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745857
Supporting Variants
Samples
Known GenesCCDC151
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296272
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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