A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3184546



Internal ID22338213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32531423..32531487hg38UCSC Ensembl
chr7:32571035..32571099hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8464n152
Supporting Variantsnssv14400659
SamplesNA19240
Known GenesAVL9
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3184546
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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