A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506037



Internal ID20879312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:134871..155584hg38UCSC Ensembl
chr16:184870..205583hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3820714
hg1920714
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197063
Samples
Known GenesHBZ, NPRL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506037
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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