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nsv5508124

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,580

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 147 SVs from 32 studies. See in: genome view    
Submitted genomic84,895,122-84,896,701Question Mark
Overlapping variant regions from other studies: 147 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):85,288,901-85,290,480Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5508124Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1284,895,12284,896,701
nsv5508124RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1285,288,90185,290,480

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17689727deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17689727Submitted genomicNC_000012.12:g.848
95122_84896701del
GRCh38 (hg38)NC_000012.12Chr1284,895,12284,896,701
nssv17689727RemappedPerfectNC_000012.11:g.852
88901_85290480del
GRCh37.p13First PassNC_000012.11Chr1285,288,90185,290,480

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)
nssv17689727<0.00116404
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