A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510526



Internal ID20883846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86460827..86462112hg38UCSC Ensembl
chr16:86494433..86495718hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg381286
hg191286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033486
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510526
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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