A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502160



Internal ID20875402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14660572..14663583hg38UCSC Ensembl
chr16:14754429..14757440hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg383012
hg193012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028470
Samples
Known GenesBFAR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502160
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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