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nsv5412230

  • 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: 94 SVs from 18 studies. See in: genome view    
Submitted genomic130,848,811-130,848,862Question Mark
Overlapping variant regions from other studies: 94 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):131,169,951-131,170,002Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5412230Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6130,848,811130,848,862
nsv5412230RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6131,169,951131,170,002

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16969743alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16969743Submitted genomicNC_000006.12:g.130
848811_130848862in
s279
GRCh38 (hg38)NC_000006.12Chr6130,848,811130,848,862
nssv16969743RemappedPerfectNC_000006.11:g.131
169951_131170002in
s279
GRCh37.p13First PassNC_000006.11Chr6131,169,951131,170,002

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)
nssv16969743<0.00116404
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