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nsv5442328

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:81

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 100 SVs from 16 studies. See in: genome view    
Submitted genomic218,448,033-218,448,113Question Mark
Overlapping variant regions from other studies: 100 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):219,312,756-219,312,836Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5442328Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2218,448,033218,448,113
nsv5442328RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2219,312,756219,312,836

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16928223deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16928223Submitted genomicNC_000002.12:g.218
448033_218448113de
l
GRCh38 (hg38)NC_000002.12Chr2218,448,033218,448,113
nssv16928223RemappedPerfectNC_000002.11:g.219
312756_219312836de
l
GRCh37.p13First PassNC_000002.11Chr2219,312,756219,312,836

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)
nssv16928223<0.00126404
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