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nsv5561671

  • 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: 294 SVs from 15 studies. See in: genome view    
Submitted genomic14,472,830-14,472,881Question Mark
Overlapping variant regions from other studies: 295 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):16,584,710-16,584,761Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5561671Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000024.10ChrY14,472,83014,472,881
nsv5561671RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000024.9ChrY16,584,71016,584,761

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17742795line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17742795Submitted genomicNC_000024.10:g.144
72830_14472881ins6
016
GRCh38 (hg38)NC_000024.10ChrY14,472,83014,472,881
nssv17742795RemappedPerfectNC_000024.9:g.1658
4710_16584761ins60
16
GRCh37.p13First PassNC_000024.9ChrY16,584,71016,584,761

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)
nssv17742795<0.00133198
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