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nsv5410260

  • 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: 90 SVs from 21 studies. See in: genome view    
Submitted genomic74,229,492-74,229,543Question Mark
Overlapping variant regions from other studies: 90 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):73,940,537-73,940,588Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5410260Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1174,229,49274,229,543
nsv5410260RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1173,940,53773,940,588

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17048384alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17048384Submitted genomicNC_000011.10:g.742
29492_74229543ins2
81
GRCh38 (hg38)NC_000011.10Chr1174,229,49274,229,543
nssv17048384RemappedPerfectNC_000011.9:g.7394
0537_73940588ins28
1
GRCh37.p13First PassNC_000011.9Chr1173,940,53773,940,588

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)
nssv170483840.01626404
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