A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522098



Internal ID20895459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3056359..3064649hg38UCSC Ensembl
chr18:3056357..3064647hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg388291
hg198291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039841
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522098
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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