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nsv4543317

  • 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: 52 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):10,363,162-10,363,162Question Mark
Overlapping variant regions from other studies: 53 SVs from 7 studies. See in: genome view    
Submitted genomic10,515,761-10,515,761Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4543317RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1210,363,16210,363,162
nsv4543317Submitted genomicGRCh37.p13Primary AssemblyNC_000012.11Chr1210,515,76110,515,761

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15997855insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15997855RemappedPerfectNC_000012.12:g.103
63162_10363163ins8
0
GRCh38.p12First PassNC_000012.12Chr1210,363,16210,363,162
nssv15997855Submitted genomicNC_000012.11:g.105
15761_10515762ins8
0
GRCh37.p13NC_000012.11Chr1210,515,76110,515,761

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)
nssv159978554.6e-005121584
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