A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920650



Internal ID22695873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35952858..35952909hg38UCSC Ensembl
chr9:35952855..35952906hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436134
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920650
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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