A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505829



Internal ID20879102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:51904619..51905257hg38UCSC Ensembl
chr16:51938530..51939168hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030356
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505829
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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