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nsv4544022

  • 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: 75 SVs from 8 studies. See in: genome view    
Remapped(Score: Perfect):38,411,100-38,411,100Question Mark
Overlapping variant regions from other studies: 77 SVs from 8 studies. See in: genome view    
Submitted genomic38,411,097-38,411,097Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4544022RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr938,411,10038,411,100
nsv4544022Submitted genomicGRCh37.p13Primary AssemblyNC_000009.11Chr938,411,09738,411,097

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16085720insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16085720RemappedPerfectNC_000009.12:g.384
11100_38411101ins5
9
GRCh38.p12First PassNC_000009.12Chr938,411,10038,411,100
nssv16085720Submitted genomicNC_000009.11:g.384
11097_38411098ins5
9
GRCh37.p13NC_000009.11Chr938,411,09738,411,097

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)
nssv160857209.2e-005221630
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