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nsv5514040

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:719

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 173 SVs from 37 studies. See in: genome view    
Submitted genomic70,249,883-70,250,601Question Mark
Overlapping variant regions from other studies: 173 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):70,283,786-70,284,504Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5514040Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1670,249,88370,250,601
nsv5514040RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1670,283,78670,284,504

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17707187deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17707187Submitted genomicNC_000016.10:g.702
49883_70250601del
GRCh38 (hg38)NC_000016.10Chr1670,249,88370,250,601
nssv17707187RemappedPerfectNC_000016.9:g.7028
3786_70284504del
GRCh37.p13First PassNC_000016.9Chr1670,283,78670,284,504

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)
nssv17707187<0.00116404
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