A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509108



Internal ID20882414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50665830..50666521hg38UCSC Ensembl
chr16:50699741..50700432hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38692
hg19692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030022
Samples
Known GenesSNX20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509108
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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