A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205977



Internal ID22354591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70450322..70450374hg38UCSC Ensembl
chr17:68446463..68446515hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3622n152
Supporting Variantsnssv14456310
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205977
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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