A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636152



Internal ID21584457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5737322..5737322hg38UCSC Ensembl
chr9:5737322..5737322hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162099
SamplesHG00096
Known GenesKIAA1432
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636152
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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