A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531909



Internal ID20905270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13188429..13195030hg38UCSC Ensembl
chr19:13299243..13305844hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg386602
hg196602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045413
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531909
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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