A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039877



Internal ID20606918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:30819692..30828028hg38UCSC Ensembl
chr18:28399658..28407994hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg388337
hg198337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532235
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039877
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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