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nsv5561908

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 87 SVs from 19 studies. See in: genome view    
Submitted genomic47,021,378-47,021,429Question Mark
Overlapping variant regions from other studies: 87 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):46,989,114-46,989,165Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5561908Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr647,021,37847,021,429
nsv5561908RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr646,989,11446,989,165

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16984835line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16984835Submitted genomicNC_000006.12:g.470
21378_47021429ins4
71
GRCh38 (hg38)NC_000006.12Chr647,021,37847,021,429
nssv16984835RemappedPerfectNC_000006.11:g.469
89114_46989165ins4
71
GRCh37.p13First PassNC_000006.11Chr646,989,11446,989,165

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)
nssv16984835<0.00126404
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