A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505574



Internal ID20878845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21724701..21729400hg38UCSC Ensembl
chr16:21736022..21740721hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186641
Samples
Known GenesOTOA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505574
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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