A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155966



Internal ID21441325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101617062..101617062hg38UCSC Ensembl
chr9:104379344..104379344hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381084
hg191084
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637865
Supporting Variants
SamplesHG00732
Known GenesGRIN3A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155966
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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