A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908135



Internal ID22683345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119214577..119214636hg38UCSC Ensembl
chr10:120974089..120974148hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360864
Samples
Known GenesGRK5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908135
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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