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nsv5547503

  • 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: 96 SVs from 24 studies. See in: genome view    
Submitted genomic141,482,755-141,482,755Question Mark
Overlapping variant regions from other studies: 94 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):140,862,322-140,862,322Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5547503Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5141,482,755141,482,755
nsv5547503RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5140,862,322140,862,322

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16975425insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16975425Submitted genomicNC_000005.10:g.141
482755_141482756in
s191
GRCh38 (hg38)NC_000005.10Chr5141,482,755141,482,755
nssv16975425RemappedPerfectNC_000005.9:g.1408
62322_140862323ins
191
GRCh37.p13First PassNC_000005.9Chr5140,862,322140,862,322

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)
nssv169754250.0835306348
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