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nsv5554911

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 264 SVs from 18 studies. See in: genome view    
Submitted genomic103,713,564-103,713,615Question Mark
Overlapping variant regions from other studies: 264 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):102,968,492-102,968,543Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5554911Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX103,713,564103,713,615
nsv5554911RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX102,968,492102,968,543

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17741789alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17741789Submitted genomicNC_000023.11:g.103
713564_103713615in
s234
GRCh38 (hg38)NC_000023.11ChrX103,713,564103,713,615
nssv17741789RemappedPerfectNC_000023.10:g.102
968492_102968543in
s234
GRCh37.p13First PassNC_000023.10ChrX102,968,492102,968,543

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)
nssv17741789<0.00126404
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