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nsv4525645

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:126,002

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 104 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):17,038,000-17,164,001Question Mark
Overlapping variant regions from other studies: 104 SVs from 14 studies. See in: genome view    
Submitted genomic17,079,999-17,206,000Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4525645RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1017,038,00017,164,001
nsv4525645Submitted genomicGRCh37.p13Primary AssemblyNC_000010.10Chr1017,079,99917,206,000

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15946110duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15946110RemappedPerfectNC_000010.11:g.170
38000_17164001dup
GRCh38.p12First PassNC_000010.11Chr1017,038,00017,164,001
nssv15946110Submitted genomicNC_000010.10:g.170
79999_17206000dup
GRCh37.p13NC_000010.10Chr1017,079,99917,206,000

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)
nssv159461104.7e-005121494
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