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nsv4577358

  • 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: 96 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):21,736,762-21,736,762Question Mark
Overlapping variant regions from other studies: 97 SVs from 6 studies. See in: genome view    
Submitted genomic23,898,648-23,898,648Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4577358RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000024.10ChrY21,736,76221,736,762
nsv4577358Submitted genomicGRCh37.p13Primary AssemblyNC_000024.9ChrY23,898,64823,898,648

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091019alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091019RemappedPerfectNC_000024.10:g.217
36762_21736763ins2
81
GRCh38.p12First PassNC_000024.10ChrY21,736,76221,736,762
nssv16091019Submitted genomicNC_000024.9:g.2389
8648_23898649ins28
1
GRCh37.p13NC_000024.9ChrY23,898,64823,898,648

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)
nssv160910190.474515510886
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