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nsv5393965

  • 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: 99 SVs from 21 studies. See in: genome view    
Submitted genomic150,711,810-150,711,861Question Mark
Overlapping variant regions from other studies: 112 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):150,684,286-150,684,337Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5393965Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1150,711,810150,711,861
nsv5393965RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1150,684,286150,684,337

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16890592alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16890592Submitted genomicNC_000001.11:g.150
711810_150711861in
s199
GRCh38 (hg38)NC_000001.11Chr1150,711,810150,711,861
nssv16890592RemappedPerfectNC_000001.10:g.150
684286_150684337in
s199
GRCh37.p13First PassNC_000001.10Chr1150,684,286150,684,337

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)
nssv16890592<0.00116404
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