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nsv5402365

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 76 SVs from 26 studies. See in: genome view    
Submitted genomic9,035,827-9,035,878Question Mark
Overlapping variant regions from other studies: 76 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):9,057,374-9,057,425Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5402365Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr119,035,8279,035,878
nsv5402365RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr119,057,3749,057,425

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17040285alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17040285Submitted genomicNC_000011.10:g.903
5827_9035878ins281
GRCh38 (hg38)NC_000011.10Chr119,035,8279,035,878
nssv17040285RemappedPerfectNC_000011.9:g.9057
374_9057425ins281
GRCh37.p13First PassNC_000011.9Chr119,057,3749,057,425

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)
nssv170402850.015976404
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