nsv5528034

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:355

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 261 SVs from 30 studies. See in: genome view    
Submitted genomic19,557,558-19,557,912Question Mark
Overlapping variant regions from other studies: 261 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):19,460,871-19,461,225Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5528034Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1719,557,55819,557,912
nsv5528034RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1719,460,87119,461,225

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17712011deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17712011Submitted genomicNC_000017.11:g.195
57558_19557912del
GRCh38 (hg38)NC_000017.11Chr1719,557,55819,557,912
nssv17712011RemappedPerfectNC_000017.10:g.194
60871_19461225del
GRCh37.p13First PassNC_000017.10Chr1719,460,87119,461,225

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)
nssv17712011<0.00116404
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