A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530606



Internal ID20903967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10959201..10962400hg38UCSC Ensembl
chr19:11069877..11073076hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198052
Samples
Known GenesSMARCA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530606
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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