A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505690



Internal ID20878963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30780611..30867997hg38UCSC Ensembl
chr16:30791932..30879318hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3887387
hg1987387
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184509
Samples
Known GenesBCL7C, ZNF629
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505690
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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