A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513579



Internal ID20886925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81469869..81475257hg38UCSC Ensembl
chr16:81503474..81508862hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg385389
hg195389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032878
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513579
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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