A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528063



Internal ID20901424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47496776..47498552hg38UCSC Ensembl
chr19:48000033..48001809hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg381777
hg191777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048298
Samples
Known GenesNAPA, NAPA-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528063
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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