A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516666



Internal ID20890027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:73591026..73666184hg38UCSC Ensembl
chr18:71258261..71333419hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3875159
hg1975159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045643
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516666
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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