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nsv5529699

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:74

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 143 SVs from 30 studies. See in: genome view    
Submitted genomic69,303,792-69,303,865Question Mark
Overlapping variant regions from other studies: 143 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):67,299,933-67,300,006Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5529699Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1769,303,79269,303,865
nsv5529699RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1767,299,93367,300,006

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714268deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714268Submitted genomicNC_000017.11:g.693
03792_69303865del
GRCh38 (hg38)NC_000017.11Chr1769,303,79269,303,865
nssv17714268RemappedPerfectNC_000017.10:g.672
99933_67300006del
GRCh37.p13First PassNC_000017.10Chr1767,299,93367,300,006

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)
nssv177142680.005336396
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