A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531495



Internal ID20904856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40448508..40452738hg38UCSC Ensembl
chr19:40954415..40958645hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg384231
hg194231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047754
Samples
Known GenesBLVRB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531495
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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