A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177620



Internal ID20744660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26820932..27062097hg38UCSC Ensembl
chr18:24400896..24642061hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38241166
hg19241166
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519394
Supporting Variants
Samples
Known GenesAQP4, AQP4-AS1, CHST9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177620
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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