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nsv5393976

  • 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: 101 SVs from 24 studies. See in: genome view    
Submitted genomic185,197,342-185,197,393Question Mark
Overlapping variant regions from other studies: 101 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):184,915,130-184,915,181Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5393976Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3185,197,342185,197,393
nsv5393976RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3184,915,130184,915,181

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16942572alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16942572Submitted genomicNC_000003.12:g.185
197342_185197393in
s107
GRCh38 (hg38)NC_000003.12Chr3185,197,342185,197,393
nssv16942572RemappedPerfectNC_000003.11:g.184
915130_184915181in
s107
GRCh37.p13First PassNC_000003.11Chr3184,915,130184,915,181

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)
nssv16942572<0.00116404
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