A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611661



Internal ID21559966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8987642..8987642hg38UCSC Ensembl
chr3:9029326..9029326hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137707
SamplesHG00512
Known GenesSRGAP3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611661
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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