A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041077



Internal ID21950413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9086726..9086726hg38UCSC Ensembl
chr3:9128410..9128410hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529420
Samples
Known GenesSRGAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041077
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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