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nsv5899764

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19,511

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 266 SVs from 50 studies. See in: genome view    
Submitted genomic181,207,147-181,226,657Question Mark
Overlapping variant regions from other studies: 266 SVs from 50 studies. See in: genome view    
Remapped(Score: Perfect):180,634,147-180,653,657Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5899764Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5181,207,147181,226,657
nsv5899764RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5180,634,147180,653,657

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17428534duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17428534Submitted genomicNC_000005.10:g.181
207147_181226657du
p
GRCh38 (hg38)NC_000005.10Chr5181,207,147181,226,657
nssv17428534RemappedPerfectNC_000005.9:g.1806
34147_180653657dup
GRCh37.p13First PassNC_000005.9Chr5180,634,147180,653,657

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)
nssv174285340.00111820
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