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nsv5394230

  • 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: 66 SVs from 14 studies. See in: genome view    
Submitted genomic154,457,432-154,457,483Question Mark
Overlapping variant regions from other studies: 66 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):153,836,992-153,837,043Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5394230Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5154,457,432154,457,483
nsv5394230RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5153,836,992153,837,043

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17735449alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17735449Submitted genomicNC_000005.10:g.154
457432_154457483in
s244
GRCh38 (hg38)NC_000005.10Chr5154,457,432154,457,483
nssv17735449RemappedPerfectNC_000005.9:g.1538
36992_153837043ins
244
GRCh37.p13First PassNC_000005.9Chr5153,836,992153,837,043

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)
nssv17735449<0.00116404
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