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nsv2791379

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,479

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 277 SVs from 56 studies. See in: genome view    
Submitted genomic90,065,915-90,077,393Question Mark
Overlapping variant regions from other studies: 277 SVs from 56 studies. See in: genome view    
Remapped(Score: Perfect):89,799,083-89,810,561Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv2791379Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1190,065,91590,077,393
nsv2791379RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1189,799,08389,810,561

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv13681788deletionSequencingGenotyping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv13681788Submitted genomicNC_000011.10:g.900
65915_90077393del1
1479
GRCh38 (hg38)NC_000011.10Chr1190,065,91590,077,393
nssv13681788RemappedPerfectNC_000011.9:g.8979
9083_89810561del11
479
GRCh37.p13First PassNC_000011.9Chr1189,799,08389,810,561

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)
nssv136817880.251560
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