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nsv5498120

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 73 SVs from 18 studies. See in: genome view    
Submitted genomic70,357,056-70,357,107Question Mark
Overlapping variant regions from other studies: 73 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):70,203,162-70,203,213Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5498120Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1170,357,05670,357,107
nsv5498120RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1170,203,16270,203,213

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17046427duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17046427Submitted genomicNC_000011.10:g.703
57056_70357107dup
GRCh38 (hg38)NC_000011.10Chr1170,357,05670,357,107
nssv17046427RemappedPerfectNC_000011.9:g.7020
3162_70203213dup
GRCh37.p13First PassNC_000011.9Chr1170,203,16270,203,213

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)
nssv170464270.00186404
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