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nsv5430748

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:291

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 143 SVs from 27 studies. See in: genome view    
Submitted genomic46,556,854-46,557,144Question Mark
Overlapping variant regions from other studies: 143 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):47,022,526-47,022,816Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5430748Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr146,556,85446,557,144
nsv5430748RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr147,022,52647,022,816

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16901876duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16901876Submitted genomicNC_000001.11:g.465
56854_46557144dup
GRCh38 (hg38)NC_000001.11Chr146,556,85446,557,144
nssv16901876RemappedPerfectNC_000001.10:g.470
22526_47022816dup
GRCh37.p13First PassNC_000001.10Chr147,022,52647,022,816

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)
nssv16901876<0.00116404
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