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nsv5453536

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:551

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 187 SVs from 34 studies. See in: genome view    
Submitted genomic48,973,387-48,973,937Question Mark
Overlapping variant regions from other studies: 187 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):49,200,526-49,201,076Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5453536Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr248,973,38748,973,937
nsv5453536RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr249,200,52649,201,076

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16913696duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16913696Submitted genomicNC_000002.12:g.489
73387_48973937dup
GRCh38 (hg38)NC_000002.12Chr248,973,38748,973,937
nssv16913696RemappedPerfectNC_000002.11:g.492
00526_49201076dup
GRCh37.p13First PassNC_000002.11Chr249,200,52649,201,076

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)
nssv169136960.0412646404
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