nsv5410009

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 98 SVs from 22 studies. See in: genome view    
Submitted genomic24,975,536-24,975,587Question Mark
Overlapping variant regions from other studies: 98 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):25,015,155-25,015,206Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5410009Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr724,975,53624,975,587
nsv5410009RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr725,015,15525,015,206

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16994192alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16994192Submitted genomicNC_000007.14:g.249
75536_24975587ins2
80
GRCh38 (hg38)NC_000007.14Chr724,975,53624,975,587
nssv16994192RemappedPerfectNC_000007.13:g.250
15155_25015206ins2
80
GRCh37.p13First PassNC_000007.13Chr725,015,15525,015,206

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv169941920.00176404
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