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nsv5504854

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:72

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 80 SVs from 14 studies. See in: genome view    
Submitted genomic103,138,428-103,138,499Question Mark
Overlapping variant regions from other studies: 80 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):104,898,185-104,898,256Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5504854Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10103,138,428103,138,499
nsv5504854RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10104,898,185104,898,256

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17039985duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17039985Submitted genomicNC_000010.11:g.103
138428_103138499du
p
GRCh38 (hg38)NC_000010.11Chr10103,138,428103,138,499
nssv17039985RemappedPerfectNC_000010.10:g.104
898185_104898256du
p
GRCh37.p13First PassNC_000010.10Chr10104,898,185104,898,256

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)
nssv17039985<0.00116404
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