A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3531765



Internal ID22401115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27884060..27884060hg38UCSC Ensembl
chr3:27925551..27925551hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14451072, nssv14423881
SamplesHG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3531765
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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