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nsv5419177

  • 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: 98 SVs from 18 studies. See in: genome view    
Submitted genomic69,606,490-69,606,541Question Mark
Overlapping variant regions from other studies: 98 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):69,640,393-69,640,444Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5419177Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1669,606,49069,606,541
nsv5419177RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1669,640,39369,640,444

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17707132alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17707132Submitted genomicNC_000016.10:g.696
06490_69606541ins2
76
GRCh38 (hg38)NC_000016.10Chr1669,606,49069,606,541
nssv17707132RemappedPerfectNC_000016.9:g.6964
0393_69640444ins27
6
GRCh37.p13First PassNC_000016.9Chr1669,640,39369,640,444

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)
nssv177071320.002116404
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