A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182020



Internal ID20749060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:30285801..30319300hg38UCSC Ensembl
chr18:27865766..27899266hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3833500
hg1933501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527687
Supporting Variants
Samples
Known GenesMIR302F
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182020
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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