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nsv5525166

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:78

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 132 SVs from 16 studies. See in: genome view    
Submitted genomic3,849,444-3,849,521Question Mark
Overlapping variant regions from other studies: 132 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):3,899,445-3,899,522Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5525166Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr163,849,4443,849,521
nsv5525166RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr163,899,4453,899,522

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17706393duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17706393Submitted genomicNC_000016.10:g.384
9444_3849521dup
GRCh38 (hg38)NC_000016.10Chr163,849,4443,849,521
nssv17706393RemappedPerfectNC_000016.9:g.3899
445_3899522dup
GRCh37.p13First PassNC_000016.9Chr163,899,4453,899,522

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)
nssv17706393<0.00126404
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