A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932235



Internal ID22707529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2599918..2678342hg38UCSC Ensembl
chr16:2649919..2728343hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3878425
hg1978425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv785n209
Supporting Variantsnssv17382668
Samples
Known GenesERVK13-1, FLJ42627, LOC652276, PDPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932235
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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