A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510051



Internal ID20883365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30582007..30634131hg38UCSC Ensembl
chr16:30593328..30645452hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3852125
hg1952125
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178936
Samples
Known GenesZNF689, ZNF785
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510051
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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