A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504196



Internal ID20877457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79643405..79648186hg38UCSC Ensembl
chr16:79677302..79682083hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg384782
hg194782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032214
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504196
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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