A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533625



Internal ID20906986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22305506..22305915hg38UCSC Ensembl
chr18:19885469..19885878hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040292
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533625
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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