A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506109



Internal ID20879385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:200292..245086hg38UCSC Ensembl
chr16:250291..295085hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3844795
hg1944795
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196477
Samples
Known GenesITFG3, LUC7L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506109
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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