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nsv5442689

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:137,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 390 SVs from 54 studies. See in: genome view    
Submitted genomic31,664,000-31,801,000Question Mark
Overlapping variant regions from other studies: 390 SVs from 54 studies. See in: genome view    
Remapped(Score: Perfect):31,889,069-32,026,069Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5442689Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr231,664,00031,801,000
nsv5442689RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr231,889,06932,026,069

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16910730deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16910730Submitted genomicNC_000002.12:g.316
64000_31801000del
GRCh38 (hg38)NC_000002.12Chr231,664,00031,801,000
nssv16910730RemappedPerfectNC_000002.11:g.318
89069_32026069del
GRCh37.p13First PassNC_000002.11Chr231,889,06932,026,069

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)
nssv16910730<0.00126404
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