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nsv4573493

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 42 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):127,062,100-127,062,100Question Mark
Overlapping variant regions from other studies: 42 SVs from 5 studies. See in: genome view    
Submitted genomic129,824,379-129,824,379Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4573493RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr9127,062,100127,062,100
nsv4573493Submitted genomicGRCh37.p13Primary AssemblyNC_000009.11Chr9129,824,379129,824,379

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16086750line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16086750RemappedPerfectNC_000009.12:g.127
062100_127062101in
s6018
GRCh38.p12First PassNC_000009.12Chr9127,062,100127,062,100
nssv16086750Submitted genomicNC_000009.11:g.129
824379_129824380in
s6018
GRCh37.p13NC_000009.11Chr9129,824,379129,824,379

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)
nssv160867504.6e-005121690
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