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nsv5506506

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:106,558

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 606 SVs from 61 studies. See in: genome view    
Submitted genomic21,455,390-21,561,947Question Mark
Overlapping variant regions from other studies: 611 SVs from 61 studies. See in: genome view    
Remapped(Score: Good):21,923,549-22,030,078Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5506506Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1421,455,39021,561,947
nsv5506506RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1421,923,54922,030,078

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17695334duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17695334Submitted genomicNC_000014.9:g.2145
5390_21561947dup
GRCh38 (hg38)NC_000014.9Chr1421,455,39021,561,947
nssv17695334RemappedGoodNC_000014.8:g.2192
3549_22030078dup
GRCh37.p13First PassNC_000014.8Chr1421,923,54922,030,078

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)
nssv17695334<0.00126404
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