A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924181



Internal ID22699408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32253190..32342825hg38UCSC Ensembl
chr9:32253188..32342823hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3889636
hg1989636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448937
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924181
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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