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nsv5413210

  • 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: 91 SVs from 19 studies. See in: genome view    
Submitted genomic44,061,233-44,061,284Question Mark
Overlapping variant regions from other studies: 91 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):44,028,970-44,029,021Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5413210Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr644,061,23344,061,284
nsv5413210RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr644,028,97044,029,021

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16984743alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16984743Submitted genomicNC_000006.12:g.440
61233_44061284ins2
81
GRCh38 (hg38)NC_000006.12Chr644,061,23344,061,284
nssv16984743RemappedPerfectNC_000006.11:g.440
28970_44029021ins2
81
GRCh37.p13First PassNC_000006.11Chr644,028,97044,029,021

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)
nssv16984743<0.00136404
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