A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205396



Internal ID22354091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95736217..95755532hg38UCSC Ensembl
chr3:95455061..95474376hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3819316
hg1919316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6074n152
Supporting Variantsnssv14434118, nssv14460442
SamplesHG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205396
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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