A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499110



Internal ID20872326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47586401..47587500hg38UCSC Ensembl
chr16:47620312..47621411hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029734
Samples
Known GenesPHKB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499110
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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