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esv2621844

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:51,290

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 456 SVs from 71 studies. See in: genome view    
Remapped(Score: Perfect):52,222,900-52,274,189Question Mark
Overlapping variant regions from other studies: 462 SVs from 71 studies. See in: genome view    
Remapped(Score: Perfect):53,982,660-54,033,949Question Mark
Overlapping variant regions from other studies: 209 SVs from 21 studies. See in: genome view    
Submitted genomic53,652,666-53,703,955Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
esv2621844RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1052,222,90052,274,189
esv2621844RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1053,982,66054,033,949
esv2621844Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000010.9Chr1053,652,66653,703,955

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5275838deletionNA18507SequencingPaired-end mapping232,775

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
essv5275838RemappedPerfectNC_000010.11:g.(52
222900_?)_(?_52274
189)del
GRCh38.p12First PassNC_000010.11Chr1052,222,90052,274,189
essv5275838RemappedPerfectNC_000010.10:g.(53
982660_?)_(?_54033
949)del
GRCh37.p13First PassNC_000010.10Chr1053,982,66054,033,949
essv5275838Submitted genomicNC_000010.9:g.(536
52666_?)_(?_537039
55)del
NCBI36 (hg18)NC_000010.9Chr1053,652,66653,703,955

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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