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nsv4658007

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21,771

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 522 SVs from 42 studies. See in: genome view    
Submitted genomic154,591,327-154,613,097Question Mark
Overlapping variant regions from other studies: 517 SVs from 42 studies. See in: genome view    
Remapped(Score: Good):153,819,590-153,841,350Question Mark
Overlapping variant regions from other studies: 69 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):2,025,306-2,047,076Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4658007Submitted genomicGRCh38.p13Primary AssemblyNC_000023.11ChrX154,591,327154,613,097
nsv4658007RemappedGoodGRCh37.p13Primary AssemblySecond PassNC_000023.10ChrX153,819,590153,841,350
nsv4658007RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003871103.3ChrX|NW_00
3871103.3
2,025,3062,047,076

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16181401inversionddPCROther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv16181401Submitted genomicNC_000023.11:g.(?_
154591327)_(154613
097_?)inv
GRCh38.p13NC_000023.11ChrX154,591,327154,613,097
nssv16181401RemappedPerfectNW_003871103.3:g.(
?_2025306)_(204707
6_?)inv
GRCh37.p13First PassNW_003871103.3ChrX|NW_00
3871103.3
2,025,3062,047,076
nssv16181401RemappedGoodNC_000023.10:g.(?_
153819590)_(153841
350_?)inv
GRCh37.p13Second PassNC_000023.10ChrX153,819,590153,841,350

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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