A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925054



Internal ID22700281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91970455..91970512hg38UCSC Ensembl
chr10:93730212..93730269hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364873
Samples
Known GenesBTAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925054
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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