A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504331



Internal ID20877592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83870238..84028738hg38UCSC Ensembl
chr16:83903843..84062343hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38158501
hg19158501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032496
Samples
Known GenesMLYCD, NECAB2, OSGIN1, SLC38A8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504331
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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