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nsv5415181

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,242

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 292 SVs from 24 studies. See in: genome view    
Submitted genomic14,831,837-14,838,078Question Mark
Overlapping variant regions from other studies: 293 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):14,849,959-14,856,200Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5415181Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX14,831,83714,838,078
nsv5415181RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX14,849,95914,856,200

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17739376deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17739376Submitted genomicNC_000023.11:g.148
31837_14838078del
GRCh38 (hg38)NC_000023.11ChrX14,831,83714,838,078
nssv17739376RemappedPerfectNC_000023.10:g.148
49959_14856200del
GRCh37.p13First PassNC_000023.10ChrX14,849,95914,856,200

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)
nssv177393760.002124805
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