A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498872



Internal ID20872086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19530539..19531859hg38UCSC Ensembl
chr16:19541861..19543181hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg381321
hg191321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028159
Samples
Known GenesCCP110
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498872
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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