A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496538



Internal ID20869741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27746001..27748100hg38UCSC Ensembl
chr16:27757322..27759421hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029297
Samples
Known GenesKIAA0556
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496538
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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