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nsv5443298

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,228

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 125 SVs from 23 studies. See in: genome view    
Submitted genomic219,268,247-219,269,474Question Mark
Overlapping variant regions from other studies: 125 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):220,132,969-220,134,196Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5443298Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2219,268,247219,269,474
nsv5443298RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2220,132,969220,134,196

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16925992deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16925992Submitted genomicNC_000002.12:g.219
268247_219269474de
l
GRCh38 (hg38)NC_000002.12Chr2219,268,247219,269,474
nssv16925992RemappedPerfectNC_000002.11:g.220
132969_220134196de
l
GRCh37.p13First PassNC_000002.11Chr2220,132,969220,134,196

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)
nssv169259920.00186404
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