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nsv5422918

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,813

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 123 SVs from 38 studies. See in: genome view    
Submitted genomic17,006,101-17,008,913Question Mark
Overlapping variant regions from other studies: 123 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):17,332,596-17,335,408Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5422918Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr117,006,10117,008,913
nsv5422918RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr117,332,59617,335,408

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16899782deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16899782Submitted genomicNC_000001.11:g.170
06101_17008913del
GRCh38 (hg38)NC_000001.11Chr117,006,10117,008,913
nssv16899782RemappedPerfectNC_000001.10:g.173
32596_17335408del
GRCh37.p13First PassNC_000001.10Chr117,332,59617,335,408

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)
nssv16899782<0.00126404
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