A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909621



Internal ID22684831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130148942..130151603hg38UCSC Ensembl
chr10:131947206..131949867hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg382662
hg192662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364816
Samples
Known GenesGLRX3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909621
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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