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nsv5527553

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,312

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 102 SVs from 31 studies. See in: genome view    
Submitted genomic48,935,497-48,937,808Question Mark
Overlapping variant regions from other studies: 102 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):49,438,754-49,441,065Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5527553Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1948,935,49748,937,808
nsv5527553RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1949,438,75449,441,065

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723939deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723939Submitted genomicNC_000019.10:g.489
35497_48937808del
GRCh38 (hg38)NC_000019.10Chr1948,935,49748,937,808
nssv17723939RemappedPerfectNC_000019.9:g.4943
8754_49441065del
GRCh37.p13First PassNC_000019.9Chr1949,438,75449,441,065

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)
nssv177239390.005316360
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