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nsv4181320

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:404,984

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 476 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):55,083,116-55,488,099Question Mark
Overlapping variant regions from other studies: 476 SVs from 18 studies. See in: genome view    
Submitted genomic56,842,876-57,247,859Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4181320RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1055,083,11655,488,099
nsv4181320Submitted genomicGRCh37.p13Primary AssemblyNC_000010.10Chr1056,842,87657,247,859

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15794116deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15794116RemappedPerfectNC_000010.11:g.550
83116_55488099del
GRCh38.p12First PassNC_000010.11Chr1055,083,11655,488,099
nssv15794116Submitted genomicNC_000010.10:g.568
42876_57247859del
GRCh37.p13NC_000010.10Chr1056,842,87657,247,859

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)
nssv157941164.6e-005121694
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