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nsv5540804

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:51

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 102 SVs from 20 studies. See in: genome view    
Submitted genomic94,465,701-94,465,751Question Mark
Overlapping variant regions from other studies: 102 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):94,932,038-94,932,088Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5540804Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1494,465,70194,465,751
nsv5540804RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1494,932,03894,932,088

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17699167insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17699167Submitted genomicNC_000014.9:g.9446
5701_94465751ins17
7
GRCh38 (hg38)NC_000014.9Chr1494,465,70194,465,751
nssv17699167RemappedPerfectNC_000014.8:g.9493
2038_94932088ins17
7
GRCh37.p13First PassNC_000014.8Chr1494,932,03894,932,088

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)
nssv17699167<0.00126404
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