A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514969



Internal ID20888324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30838778..30846059hg38UCSC Ensembl
chr16:30850099..30857380hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg387282
hg197282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029193
Samples
Known GenesBCL7C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514969
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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