A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506674



Internal ID20879958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11472892..11537099hg38UCSC Ensembl
chr16:11566748..11630955hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3864208
hg1964208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2689n223
Supporting Variantsnssv18028352
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506674
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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