A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924377



Internal ID22699604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123203750..123204237hg38UCSC Ensembl
chr9:125966029..125966516hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38488
hg19488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434876
Samples
Known GenesSTRBP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924377
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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