A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3535696



Internal ID22404937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8987641..8987641hg38UCSC Ensembl
chr3:9029325..9029325hg19UCSC 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 Variantsnssv14395817
SamplesNA19240
Known GenesSRGAP3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3535696
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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