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nsv5440681

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:620

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 121 SVs from 16 studies. See in: genome view    
Submitted genomic202,291,002-202,291,621Question Mark
Overlapping variant regions from other studies: 121 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):203,155,725-203,156,344Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5440681Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2202,291,002202,291,621
nsv5440681RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2203,155,725203,156,344

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16922900deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16922900Submitted genomicNC_000002.12:g.202
291002_202291621de
l
GRCh38 (hg38)NC_000002.12Chr2202,291,002202,291,621
nssv16922900RemappedPerfectNC_000002.11:g.203
155725_203156344de
l
GRCh37.p13First PassNC_000002.11Chr2203,155,725203,156,344

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)
nssv16922900<0.00126404
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