esv2425283

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 47 SVs from 12 studies. See in: genome view    
Remapped(Score: Perfect):122,854,889-122,854,889Question Mark
Overlapping variant regions from other studies: 47 SVs from 12 studies. See in: genome view    
Remapped(Score: Perfect):124,614,405-124,614,405Question Mark
Overlapping variant regions from other studies: 42 SVs from 9 studies. See in: genome view    
Submitted genomic124,604,395-124,604,395Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
esv2425283RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000010.11Chr10122,854,889122,854,889
esv2425283RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000010.10Chr10124,614,405124,614,405
esv2425283Submitted genomicNCBI36 (hg18)NC_000010.9Chr10124,604,395124,604,395

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5347720insertionNA18507SequencingSplit read mapping232,775

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrStartStop
essv5347720RemappedPerfectNC_000010.11:g.122
854888_122854889in
s(0_?)
GRCh38 (hg38)Primary AssemblyFirst PassNC_000010.11Chr10122,854,889122,854,889
essv5347720RemappedPerfectNC_000010.10:g.124
614404_124614405in
s(0_?)
GRCh37 (hg19)Primary AssemblyFirst PassNC_000010.10Chr10124,614,405124,614,405
essv5347720Submitted genomicNC_000010.9:g.1246
04394_124604395ins
(0_?)
NCBI36 (hg18)NC_000010.9Chr10124,604,395124,604,395

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