A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284942



Internal ID20494160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30556875..30556875hg38UCSC Ensembl
chr19:31047782..31047782hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754505
Supporting Variants
Samples
Known GenesZNF536
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284942
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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