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nsv5457080

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:236

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 81 SVs from 11 studies. See in: genome view    
Submitted genomic72,191,726-72,191,961Question Mark
Overlapping variant regions from other studies: 81 SVs from 11 studies. See in: genome view    
Remapped(Score: Perfect):71,487,553-71,487,788Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5457080Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr572,191,72672,191,961
nsv5457080RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr571,487,55371,487,788

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16967504deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16967504Submitted genomicNC_000005.10:g.721
91726_72191961del
GRCh38 (hg38)NC_000005.10Chr572,191,72672,191,961
nssv16967504RemappedPerfectNC_000005.9:g.7148
7553_71487788del
GRCh37.p13First PassNC_000005.9Chr571,487,55371,487,788

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)
nssv16967504<0.00116404
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