A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505435



Internal ID20878704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8426401..8463900hg38UCSC Ensembl
chr16:8476403..8513902hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3837500
hg1937500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032973
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505435
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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