A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326190



Internal ID20859324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22211637..22213702hg38UCSC Ensembl
chr1:22538130..22540195hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg382066
hg192066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058641
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326190
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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