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nsv5510194

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:57

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 73 SVs from 20 studies. See in: genome view    
Submitted genomic48,652,519-48,652,575Question Mark
Overlapping variant regions from other studies: 73 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):49,046,302-49,046,358Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5510194Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1248,652,51948,652,575
nsv5510194RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1249,046,30249,046,358

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058182deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058182Submitted genomicNC_000012.12:g.486
52519_48652575del
GRCh38 (hg38)NC_000012.12Chr1248,652,51948,652,575
nssv17058182RemappedPerfectNC_000012.11:g.490
46302_49046358del
GRCh37.p13First PassNC_000012.11Chr1249,046,30249,046,358

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)
nssv17058182<0.00116404
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