A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320775



Internal ID20853876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89621219..89623455hg38UCSC Ensembl
chr1:90086778..90089014hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg382237
hg192237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064941
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320775
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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