A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529221



Internal ID20902582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11039927..11040438hg38UCSC Ensembl
chr19:11150603..11151114hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198053
Samples
Known GenesSMARCA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529221
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer