A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3182295



Internal ID22337020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:82259963..82270217hg38UCSC Ensembl
chr6:82969680..82979934hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3810255
hg1910255
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7994n152
Supporting Variantsnssv14465305
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)nsv3182295
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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