esv2422275

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:153,039

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 344 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):161,628,725-161,781,763Question Mark
Overlapping variant regions from other studies: 344 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):162,049,757-162,202,795Question Mark
Overlapping variant regions from other studies: 51 SVs from 9 studies. See in: genome view    
Submitted genomic162,020,168-162,173,206Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2422275RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000006.12Chr6161,628,725161,781,763
esv2422275RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000006.11Chr6162,049,757162,202,795
esv2422275Submitted genomicNCBI35 (hg17)NC_000006.9Chr6162,020,168162,173,206

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5161358duplicationND05536SNP arraySNP genotyping analysisessv5161244, essv5161463, essv5161432

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
essv5161358RemappedPerfectNC_000006.12:g.(?_
161628725)_(161781
763_?)dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000006.12Chr6161,628,725161,781,763
essv5161358RemappedPerfectNC_000006.11:g.(?_
162049757)_(162202
795_?)dup
GRCh37 (hg19)Primary AssemblyFirst PassNC_000006.11Chr6162,049,757162,202,795
essv5161358Submitted genomicNC_000006.9:g.(?_1
62020168)_(1621732
06_?)dup
NCBI35 (hg17)NC_000006.9Chr6162,020,168162,173,206

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
essv51613582ND05536qPCROtherPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant