A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501977



Internal ID20875217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69055927..69063352hg38UCSC Ensembl
chr16:69089830..69097255hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg387426
hg197426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031758
Samples
Known GenesTANGO6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501977
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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