A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624929



Internal ID21573234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35657732..35657732hg38UCSC Ensembl
chr9:35657729..35657729hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161718
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624929
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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