A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509632



Internal ID20882943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24425457..24450724hg38UCSC Ensembl
chr16:24436778..24462045hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3825268
hg1925268
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177169
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509632
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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