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nsv5449665

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:110,896

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 418 SVs from 59 studies. See in: genome view    
Submitted genomic151,660,998-151,771,893Question Mark
Overlapping variant regions from other studies: 418 SVs from 59 studies. See in: genome view    
Remapped(Score: Perfect):151,378,786-151,489,681Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5449665Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3151,660,998151,771,893
nsv5449665RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3151,378,786151,489,681

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16941188deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16941188Submitted genomicNC_000003.12:g.151
660998_151771893de
l
GRCh38 (hg38)NC_000003.12Chr3151,660,998151,771,893
nssv16941188RemappedPerfectNC_000003.11:g.151
378786_151489681de
l
GRCh37.p13First PassNC_000003.11Chr3151,378,786151,489,681

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)
nssv16941188<0.00116404
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