A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950819



Internal ID22726211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224407143..224407143hg38UCSC Ensembl
chr1:224594845..224594845hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367953
Samples
Known GenesWDR26
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950819
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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