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nsv5452734

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,279

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 252 SVs from 38 studies. See in: genome view    
Submitted genomic196,295,030-196,299,308Question Mark
Overlapping variant regions from other studies: 252 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):196,021,901-196,026,179Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5452734Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3196,295,030196,299,308
nsv5452734RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3196,021,901196,026,179

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16944616deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16944616Submitted genomicNC_000003.12:g.196
295030_196299308de
l
GRCh38 (hg38)NC_000003.12Chr3196,295,030196,299,308
nssv16944616RemappedPerfectNC_000003.11:g.196
021901_196026179de
l
GRCh37.p13First PassNC_000003.11Chr3196,021,901196,026,179

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)
nssv16944616<0.00116404
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