A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522663



Internal ID20896024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:71398484..71430874hg38UCSC Ensembl
chr18:69065720..69098110hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3832391
hg1932391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042826
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522663
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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