A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511592



Internal ID20884921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2883204..2886489hg38UCSC Ensembl
chr16:2933205..2936490hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg383286
hg193286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029050
Samples
Known GenesFLYWCH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511592
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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