A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18042078



Internal ID20609118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:42468977..42469527hg38UCSC Ensembl
chr18:40048942..40049492hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522389
Supporting Variants
Samples
Known GenesLINC00907
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18042078
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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