A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515234



Internal ID20888593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80566499..80567501hg38UCSC Ensembl
chr16:80600396..80601398hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg381003
hg191003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032285
Samples
Known GenesLOC101928276
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515234
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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