A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187700



Internal ID20754740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11630884..11659326hg38UCSC Ensembl
chr18:11630883..11659325hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3828443
hg1928443
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526868
Supporting Variants
Samples
Known GenesMIR7153
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187700
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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