A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927816



Internal ID22703048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4253667..4253751hg38UCSC Ensembl
chr16:4303668..4303752hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375235
Samples
Known GenesLOC100507501
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927816
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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