A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514980



Internal ID20888335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52595432..52596100hg38UCSC Ensembl
chr16:52629344..52630012hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030402
Samples
Known GenesCASC16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514980
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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