A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514902



Internal ID20888257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82067974..82068580hg38UCSC Ensembl
chr16:82101579..82102185hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032607
Samples
Known GenesHSD17B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514902
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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