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nsv5481996

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:110

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 110 SVs from 33 studies. See in: genome view    
Submitted genomic56,106,327-56,106,436Question Mark
Overlapping variant regions from other studies: 110 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):56,174,020-56,174,129Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5481996Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr756,106,32756,106,436
nsv5481996RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr756,174,02056,174,129

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16996436deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16996436Submitted genomicNC_000007.14:g.561
06327_56106436del
GRCh38 (hg38)NC_000007.14Chr756,106,32756,106,436
nssv16996436RemappedPerfectNC_000007.13:g.561
74020_56174129del
GRCh37.p13First PassNC_000007.13Chr756,174,02056,174,129

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)
nssv16996436<0.00126404
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