A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496348



Internal ID20869549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30176110..30177893hg38UCSC Ensembl
chr16:30187431..30189214hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381784
hg191784
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183748
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496348
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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