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nsv4578225

  • 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: 29 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):109,247,897-109,247,897Question Mark
Overlapping variant regions from other studies: 29 SVs from 7 studies. See in: genome view    
Submitted genomic109,685,702-109,685,702Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4578225RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr12109,247,897109,247,897
nsv4578225Submitted genomicGRCh37.p13Primary AssemblyNC_000012.11Chr12109,685,702109,685,702

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16002842sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16002842RemappedPerfectNC_000012.12:g.109
247897_109247898in
s305
GRCh38.p12First PassNC_000012.12Chr12109,247,897109,247,897
nssv16002842Submitted genomicNC_000012.11:g.109
685702_109685703in
s305
GRCh37.p13NC_000012.11Chr12109,685,702109,685,702

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)
nssv160028424.6e-005121694
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