A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509553



Internal ID20882863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24909649..24911216hg38UCSC Ensembl
chr16:24920970..24922537hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381568
hg191568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029493
Samples
Known GenesSLC5A11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509553
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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