A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178889



Internal ID20745929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10379249..10533407hg38UCSC Ensembl
chr18:10379246..10533404hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38154159
hg19154159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533384
Supporting Variants
Samples
Known GenesAPCDD1, NAPG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178889
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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