A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944802



Internal ID22720272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50158045..50158366hg38UCSC Ensembl
chr16:50191956..50192277hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375145
Samples
Known GenesPAPD5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944802
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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