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nsv5466148

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,822

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 204 SVs from 42 studies. See in: genome view    
Submitted genomic181,208,731-181,218,552Question Mark
Overlapping variant regions from other studies: 204 SVs from 42 studies. See in: genome view    
Remapped(Score: Perfect):180,635,731-180,645,552Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5466148Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5181,208,731181,218,552
nsv5466148RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5180,635,731180,645,552

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16977884deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16977884Submitted genomicNC_000005.10:g.181
208731_181218552de
l
GRCh38 (hg38)NC_000005.10Chr5181,208,731181,218,552
nssv16977884RemappedPerfectNC_000005.9:g.1806
35731_180645552del
GRCh37.p13First PassNC_000005.9Chr5180,635,731180,645,552

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)
nssv16977884<0.00116404
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