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nsv5436158

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,638

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 222 SVs from 47 studies. See in: genome view    
Submitted genomic107,282,728-107,287,365Question Mark
Overlapping variant regions from other studies: 222 SVs from 47 studies. See in: genome view    
Remapped(Score: Perfect):107,899,184-107,903,821Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5436158Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2107,282,728107,287,365
nsv5436158RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2107,899,184107,903,821

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16918652deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16918652Submitted genomicNC_000002.12:g.107
282728_107287365de
l
GRCh38 (hg38)NC_000002.12Chr2107,282,728107,287,365
nssv16918652RemappedPerfectNC_000002.11:g.107
899184_107903821de
l
GRCh37.p13First PassNC_000002.11Chr2107,899,184107,903,821

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)
nssv169186520.015966404
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