A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930341



Internal ID22705606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12318717..12336177hg38UCSC Ensembl
chr16:12412574..12430034hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3817461
hg1917461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv794n209
Supporting Variantsnssv17386951
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930341
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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