A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501389



Internal ID20874622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26302404..26312814hg38UCSC Ensembl
chr16:26313725..26324135hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3810411
hg1910411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2737n223
Supporting Variantsnssv18028591
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501389
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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