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nsv5558582

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 75 SVs from 17 studies. See in: genome view    
Submitted genomic75,819,021-75,819,072Question Mark
Overlapping variant regions from other studies: 75 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):75,530,066-75,530,117Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5558582Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1175,819,02175,819,072
nsv5558582RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1175,530,06675,530,117

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17688412sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17688412Submitted genomicNC_000011.10:g.758
19021_75819072ins1
302
GRCh38 (hg38)NC_000011.10Chr1175,819,02175,819,072
nssv17688412RemappedPerfectNC_000011.9:g.7553
0066_75530117ins13
02
GRCh37.p13First PassNC_000011.9Chr1175,530,06675,530,117

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)
nssv17688412<0.00126404
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