esv2422504

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:133,337

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 357 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):82,000,723-82,134,059Question Mark
Overlapping variant regions from other studies: 357 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):82,293,064-82,426,400Question Mark
Overlapping variant regions from other studies: 31 SVs from 6 studies. See in: genome view    
Submitted genomic80,080,119-80,213,455Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2422504RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000015.10Chr1582,000,72382,134,059
esv2422504RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000015.9Chr1582,293,06482,426,400
esv2422504Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000015.8Chr1580,080,11980,213,455

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysis
essv5161251duplicationND04302SNP arraySNP genotyping analysis

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv5161251RemappedPerfectNC_000015.10:g.(?_
82000723)_(8213405
9_?)dup
GRCh38 (hg38)First PassNC_000015.10Chr1582,000,72382,134,059
essv5161251RemappedPerfectNC_000015.9:g.(?_8
2293064)_(82426400
_?)dup
GRCh37 (hg19)First PassNC_000015.9Chr1582,293,06482,426,400
essv5161251Submitted genomicNC_000015.8:g.(?_8
0080119)_(80213455
_?)dup
NCBI35 (hg17)NC_000015.8Chr1580,080,11980,213,455

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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