esv2422509

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:148,471

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 326 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):63,515,793-63,664,263Question Mark
Overlapping variant regions from other studies: 326 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):63,501,469-63,649,939Question Mark
Overlapping variant regions from other studies: 31 SVs from 6 studies. See in: genome view    
Submitted genomic63,476,509-63,624,979Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2422509RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000003.12Chr363,515,79363,664,263
esv2422509RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000003.11Chr363,501,46963,649,939
esv2422509Submitted genomicNCBI35 (hg17)NC_000003.9Chr363,476,50963,624,979

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5161261deletionND04575SNP arraySNP genotyping analysisessv5161405, essv5161335

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
essv5161261RemappedPerfectNC_000003.12:g.(?_
63515793)_(6366426
3_?)del
GRCh38 (hg38)Primary AssemblyFirst PassNC_000003.12Chr363,515,79363,664,263
essv5161261RemappedPerfectNC_000003.11:g.(?_
63501469)_(6364993
9_?)del
GRCh37 (hg19)Primary AssemblyFirst PassNC_000003.11Chr363,501,46963,649,939
essv5161261Submitted genomicNC_000003.9:g.(?_6
3476509)_(63624979
_?)del
NCBI35 (hg17)NC_000003.9Chr363,476,50963,624,979

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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