A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159765



Internal ID21498984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127182388..127182388hg38UCSC Ensembl
chr9:129944667..129944667hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5627547
Supporting Variants
SamplesNA19239
Known GenesRALGPS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159765
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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