A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969294



Internal ID22744229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8425820..8425820hg38UCSC Ensembl
chr18:8425818..8425818hg19UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17407738
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969294
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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