A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940413



Internal ID22715822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19707806..19707912hg38UCSC Ensembl
chr16:19719128..19719234hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375447
Samples
Known GenesKNOP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940413
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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