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nsv5436109

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:63

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 82 SVs from 16 studies. See in: genome view    
Submitted genomic69,602,311-69,602,373Question Mark
Overlapping variant regions from other studies: 82 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):69,829,443-69,829,505Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5436109Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr269,602,31169,602,373
nsv5436109RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr269,829,44369,829,505

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16913994deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16913994Submitted genomicNC_000002.12:g.696
02311_69602373del
GRCh38 (hg38)NC_000002.12Chr269,602,31169,602,373
nssv16913994RemappedPerfectNC_000002.11:g.698
29443_69829505del
GRCh37.p13First PassNC_000002.11Chr269,829,44369,829,505

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)
nssv16913994<0.00136404
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