A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915375



Internal ID22690593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124797947..124815331hg38UCSC Ensembl
chr10:126486516..126503900hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3817385
hg1917385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366716
Samples
Known GenesFAM175B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915375
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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