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nsv4974890

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:28,528

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 160 SVs from 46 studies. See in: genome view    
Submitted genomic122,631,326-122,659,866Question Mark
Overlapping variant regions from other studies: 160 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):125,393,605-125,422,145Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4974890Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9122,631,334 (-8, +8)122,659,861 (-5, +5)
nsv4974890RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9125,393,613 (-8, +8)125,422,140 (-5, +5)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16516750duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16516750Submitted genomicNC_000009.12:g.(12
2631326_122631342)
_(122659856_122659
866)dup
GRCh38 (hg38)NC_000009.12Chr9122,631,334 (-8, +8)122,659,861 (-5, +5)
nssv16516750RemappedPerfectNC_000009.11:g.(12
5393605_125393621)
_(125422135_125422
145)dup
GRCh37.p13First PassNC_000009.11Chr9125,393,613 (-8, +8)125,422,140 (-5, +5)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16516750<0.0011129246
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