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nsv6160860

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:66

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 115 SVs from 25 studies. See in: genome view    
Submitted genomic190,856,222-190,856,287Question Mark
Overlapping variant regions from other studies: 115 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):190,574,011-190,574,076Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6160860Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3190,856,222190,856,287
nsv6160860RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3190,574,011190,574,076

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17878956deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17878956Submitted genomicNC_000003.12:g.190
856222_190856287de
l
GRCh38 (hg38)NC_000003.12Chr3190,856,222190,856,287
nssv17878956RemappedPerfectNC_000003.11:g.190
574011_190574076de
l
GRCh37.p13First PassNC_000003.11Chr3190,574,011190,574,076

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)
nssv17878956<0.00122238
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