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nsv4578052

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 312 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):32,304,657-32,304,657Question Mark
Overlapping variant regions from other studies: 313 SVs from 6 studies. See in: genome view    
Submitted genomic32,322,774-32,322,774Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4578052RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX32,304,65732,304,657
nsv4578052Submitted genomicGRCh37.p13Primary AssemblyNC_000023.10ChrX32,322,77432,322,774

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16089543alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16089543RemappedPerfectNC_000023.11:g.323
04657_32304658ins2
81
GRCh38.p12First PassNC_000023.11ChrX32,304,65732,304,657
nssv16089543Submitted genomicNC_000023.10:g.323
22774_32322775ins2
81
GRCh37.p13NC_000023.10ChrX32,322,77432,322,774

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)
nssv160895434.6e-005121648
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