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nsv5473760

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:224

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 99 SVs from 25 studies. See in: genome view    
Submitted genomic158,984,450-158,984,673Question Mark
Overlapping variant regions from other studies: 99 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):159,405,482-159,405,705Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5473760Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6158,984,450158,984,673
nsv5473760RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6159,405,482159,405,705

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16989546deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16989546Submitted genomicNC_000006.12:g.158
984450_158984673de
l
GRCh38 (hg38)NC_000006.12Chr6158,984,450158,984,673
nssv16989546RemappedPerfectNC_000006.11:g.159
405482_159405705de
l
GRCh37.p13First PassNC_000006.11Chr6159,405,482159,405,705

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)
nssv16989546<0.00116404
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