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nsv4561882

  • 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: 107 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):26,507,258-26,507,258Question Mark
Overlapping variant regions from other studies: 108 SVs from 7 studies. See in: genome view    
Submitted genomic28,653,405-28,653,405Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4561882RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000024.10ChrY26,507,25826,507,258
nsv4561882Submitted genomicGRCh37.p13Primary AssemblyNC_000024.9ChrY28,653,40528,653,405

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091021line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091021RemappedPerfectNC_000024.10:g.265
07258_26507259ins6
019
GRCh38.p12First PassNC_000024.10ChrY26,507,25826,507,258
nssv16091021Submitted genomicNC_000024.9:g.2865
3405_28653406ins60
19
GRCh37.p13NC_000024.9ChrY28,653,40528,653,405

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)
nssv16091021<0.001311056
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