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nsv5526966

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:373

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 143 SVs from 26 studies. See in: genome view    
Submitted genomic50,766,757-50,767,129Question Mark
Overlapping variant regions from other studies: 142 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):48,844,118-48,844,490Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5526966Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1750,766,75750,767,129
nsv5526966RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1748,844,11848,844,490

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17724723deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17724723Submitted genomicNC_000017.11:g.507
66757_50767129del
GRCh38 (hg38)NC_000017.11Chr1750,766,75750,767,129
nssv17724723RemappedPerfectNC_000017.10:g.488
44118_48844490del
GRCh37.p13First PassNC_000017.10Chr1748,844,11848,844,490

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)
nssv177247230.031916404
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