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nsv590336

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,927

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 403 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):52,999,041-53,004,967Question Mark
Overlapping variant regions from other studies: 402 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):53,033,057-53,038,983Question Mark
Overlapping variant regions from other studies: 181 SVs from 24 studies. See in: genome view    
Submitted genomic53,008,097-53,014,023Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv590336RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr352,999,04153,004,967
nsv590336RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr353,033,05753,038,983
nsv590336Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000003.10Chr353,008,09753,014,023

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv963286copy number lossSNP arraySNP genotyping analysis

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv963286RemappedPerfectNC_000003.12:g.(?_
52999041)_(5300496
7_?)del
GRCh38.p12First PassNC_000003.12Chr352,999,04153,004,967
nssv963286RemappedPerfectNC_000003.11:g.(?_
53033057)_(5303898
3_?)del
GRCh37.p13First PassNC_000003.11Chr353,033,05753,038,983
nssv963286Submitted genomicNC_000003.10:g.(?_
53008097)_(5301402
3_?)del
NCBI36 (hg18)NC_000003.10Chr353,008,09753,014,023

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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