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nsv4872978

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:322

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 380 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):71,198,630-71,198,951Question Mark
Overlapping variant regions from other studies: 380 SVs from 28 studies. See in: genome view    
Submitted genomic70,418,480-70,418,801Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4872978RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX71,198,63071,198,951
nsv4872978Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000023.10ChrX70,418,48070,418,801

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16311293alu deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16311293RemappedPerfectNC_000023.11:g.711
98630_71198951del
GRCh38.p12First PassNC_000023.11ChrX71,198,63071,198,951
nssv16311293Submitted genomicNC_000023.10:g.704
18480_70418801del
GRCh37 (hg19)NC_000023.10ChrX70,418,48070,418,801

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16311293<0.001116834
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