A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935270



Internal ID22710609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2993828..2994376hg38UCSC Ensembl
chr16:3043829..3044377hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372289
Samples
Known GenesLINC00514
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935270
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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