A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908111



Internal ID22683321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127501681..127502635hg38UCSC Ensembl
chr9:130263960..130264914hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38955
hg19955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444552
Samples
Known GenesLRSAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908111
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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