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nsv5380707

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,771,982

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 10558 SVs from 131 studies. See in: genome view    
Remapped(Score: Pass):18,339,130-21,111,111Question Mark
Overlapping variant regions from other studies: 9842 SVs from 128 studies. See in: genome view    
Submitted genomic18,912,300-21,465,400Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv5380707RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000022.11Chr2218,339,13021,111,111
nsv5380707Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000022.10Chr2218,912,30021,465,400

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysis
nssv16865864deletionpsh02-LARSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv16865864RemappedPassNC_000022.11:g.(?_
18339130)_(2111111
1_?)del
GRCh38.p12First PassNC_000022.11Chr2218,339,13021,111,111
nssv16865864Submitted genomicNC_000022.10:g.(?_
18912300)_(2146540
0_?)del
GRCh37 (hg19)NC_000022.10Chr2218,912,30021,465,400

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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