A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159732



Internal ID21472014
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 StatusS
Merged Variantsnsv5593031
Supporting Variants
SamplesHG03125
Known GenesNR6A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159732
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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