A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513708



Internal ID20887055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13195876..13198474hg38UCSC Ensembl
chr16:13289733..13292331hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg382599
hg192599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028765
Samples
Known GenesSHISA9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513708
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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