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nsv5562447

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:60

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 146 SVs from 35 studies. See in: genome view    
Submitted genomic155,147,381-155,147,440Question Mark
Overlapping variant regions from other studies: 153 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):155,119,857-155,119,916Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5562447Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1155,147,381155,147,440
nsv5562447RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1155,119,857155,119,916

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16890435inversionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16890435Submitted genomicNC_000001.11:g.155
147381_155147440in
v
GRCh38 (hg38)NC_000001.11Chr1155,147,381155,147,440
nssv16890435RemappedPerfectNC_000001.10:g.155
119857_155119916in
v
GRCh37.p13First PassNC_000001.10Chr1155,119,857155,119,916

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)
nssv168904350.49931946404
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