A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500208



Internal ID20873433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19722046..19722441hg38UCSC Ensembl
chr16:19733368..19733763hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028166
Samples
Known GenesIQCK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500208
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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