A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503972



Internal ID20877230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58174881..58175294hg38UCSC Ensembl
chr16:58208785..58209198hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184915
Samples
Known GenesCSNK2A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503972
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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