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nsv6223371

  • 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: 112 SVs from 23 studies. See in: genome view    
Submitted genomic190,856,485-190,856,485Question Mark
Overlapping variant regions from other studies: 112 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):190,574,274-190,574,274Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6223371Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3190,856,485190,856,485
nsv6223371RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3190,574,274190,574,274

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17867838insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17867838Submitted genomicNC_000003.12:g.190
856485_190856486in
s56
GRCh38 (hg38)NC_000003.12Chr3190,856,485190,856,485
nssv17867838RemappedPerfectNC_000003.11:g.190
574274_190574275in
s56
GRCh37.p13First PassNC_000003.11Chr3190,574,274190,574,274

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)
nssv17867838<0.00112030
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