A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514133



Internal ID20887485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:49138175..49144424hg38UCSC Ensembl
chr16:49172086..49178335hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg386250
hg196250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514133
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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