A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500994



Internal ID20874224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4576960..4581351hg38UCSC Ensembl
chr16:4626961..4631352hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg384392
hg194392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029659
Samples
Known GenesC16orf96
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500994
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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