A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190096



Internal ID20757136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21822053..21827015hg38UCSC Ensembl
chr18:19402014..19406976hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg384963
hg194963
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517191
Supporting Variants
Samples
Known GenesMIB1, MIR133A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190096
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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