A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3173211



Internal ID22332207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:30987325..30987394hg38UCSC Ensembl
chr6:30955102..30955171hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7807n152
Supporting Variantsnssv14460024
SamplesHG00733
Known GenesMUC21
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3173211
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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