A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499255



Internal ID20872473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11747777..11748899hg38UCSC Ensembl
chr16:11841633..11842755hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg381123
hg191123
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183454
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499255
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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