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nsv5472571

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:75

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 93 SVs from 25 studies. See in: genome view    
Submitted genomic27,146,409-27,146,483Question Mark
Overlapping variant regions from other studies: 93 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):27,114,188-27,114,262Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5472571Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr627,146,40927,146,483
nsv5472571RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr627,114,18827,114,262

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16982435deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16982435Submitted genomicNC_000006.12:g.271
46409_27146483del
GRCh38 (hg38)NC_000006.12Chr627,146,40927,146,483
nssv16982435RemappedPerfectNC_000006.11:g.271
14188_27114262del
GRCh37.p13First PassNC_000006.11Chr627,114,18827,114,262

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)
nssv16982435<0.00116404
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