A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531907



Internal ID20905268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45807130..45809490hg38UCSC Ensembl
chr19:46310388..46312748hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg382361
hg192361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046531
Samples
Known GenesRSPH6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531907
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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