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nsv4498207

  • 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: 35 SVs from 4 studies. See in: genome view    
Remapped(Score: Perfect):60,938,479-60,938,479Question Mark
Overlapping variant regions from other studies: 35 SVs from 4 studies. See in: genome view    
Submitted genomic61,851,038-61,851,038Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4498207RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr860,938,47960,938,479
nsv4498207Submitted genomicGRCh37.p13Primary AssemblyNC_000008.10Chr861,851,03861,851,038

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16081474alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16081474RemappedPerfectNC_000008.11:g.609
38479_60938480ins2
81
GRCh38.p12First PassNC_000008.11Chr860,938,47960,938,479
nssv16081474Submitted genomicNC_000008.10:g.618
51038_61851039ins2
81
GRCh37.p13NC_000008.10Chr861,851,03861,851,038

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)
nssv160814744.6e-005121694
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