A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3175288



Internal ID22333276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:97227592..97227848hg38UCSC Ensembl
chr6:97675468..97675724hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38257
hg19257
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14464979
SamplesHG00733
Known GenesMIR548H3, MMS22L
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3175288
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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