A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916215



Internal ID22691434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124568446..124569075hg38UCSC Ensembl
chr9:127330725..127331354hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430681
Samples
Known GenesNR6A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916215
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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