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nsv5553785

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 112 SVs from 32 studies. See in: genome view    
Submitted genomic37,611,748-37,611,799Question Mark
Overlapping variant regions from other studies: 127 SVs from 43 studies. See in: genome view    
Remapped(Score: Pass):38,077,349-38,077,471Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5553785Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr137,611,74837,611,799
nsv5553785RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr138,077,34938,077,471

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16902051insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16902051Submitted genomicNC_000001.11:g.376
11748_37611799ins7
1
GRCh38 (hg38)NC_000001.11Chr137,611,74837,611,799
nssv16902051RemappedPassNC_000001.10:g.380
77349_38077471ins7
1
GRCh37.p13First PassNC_000001.10Chr138,077,34938,077,471

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)
nssv169020510.1710906398
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