A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504920



Internal ID20878184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26482822..26487660hg38UCSC Ensembl
chr16:26494143..26498981hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg384839
hg194839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029220
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504920
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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