nsv5530832

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,674

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 136 SVs from 26 studies. See in: genome view    
Submitted genomic69,315,198-69,317,871Question Mark
Overlapping variant regions from other studies: 136 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):67,311,339-67,314,012Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5530832Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1769,315,19869,317,871
nsv5530832RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1767,311,33967,314,012

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714270deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714270Submitted genomicNC_000017.11:g.693
15198_69317871del
GRCh38 (hg38)NC_000017.11Chr1769,315,19869,317,871
nssv17714270RemappedPerfectNC_000017.10:g.673
11339_67314012del
GRCh37.p13First PassNC_000017.10Chr1767,311,33967,314,012

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)
nssv17714270<0.00116404
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