A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507023



Internal ID20880311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30448382..30451355hg38UCSC Ensembl
chr16:30459703..30462676hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg382974
hg192974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029158
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507023
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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