A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949856



Internal ID22725295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101551616..101551616hg38UCSC Ensembl
chr9:104313898..104313898hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436732
Samples
Known GenesRNF20
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949856
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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