esv5447

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:200

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 77 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):76,751,346-76,751,545Question Mark
Overlapping variant regions from other studies: 77 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):79,366,262-79,366,461Question Mark
Overlapping variant regions from other studies: 46 SVs from 9 studies. See in: genome view    
Submitted genomic78,556,082-78,556,281Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv5447RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000009.12Chr976,751,34676,751,39076,751,48376,751,545
esv5447RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000009.11Chr979,366,26279,366,30679,366,39979,366,461
esv5447Submitted genomicNCBI36 (hg18)NC_000009.10Chr978,556,08278,556,12678,556,21978,556,281

Variant Call Information

Variant Call IDTypeMethodAnalysis
essv27888copy number gainSequencingRead depth and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv27888RemappedPerfectNC_000009.12:g.(76
751346_76751390)_(
76751483_76751545)
dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000009.12Chr976,751,34676,751,39076,751,48376,751,545
essv27888RemappedPerfectNC_000009.11:g.(79
366262_79366306)_(
79366399_79366461)
dup
GRCh37 (hg19)Primary AssemblyFirst PassNC_000009.11Chr979,366,26279,366,30679,366,39979,366,461
essv27888Submitted genomicNC_000009.10:g.(78
556082_78556126)_(
78556219_78556281)
dup
NCBI36 (hg18)NC_000009.10Chr978,556,08278,556,12678,556,21978,556,281

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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