A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504899



Internal ID20878163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3672377..3718393hg38UCSC Ensembl
chr16:3722378..3768394hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3846017
hg1946017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029418
Samples
Known GenesTRAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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