A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503953



Internal ID20877211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30874236..30877631hg38UCSC Ensembl
chr16:30885557..30888952hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg383396
hg193396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029194
Samples
Known GenesBCL7C, MIR4519
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503953
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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