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nsv5395648

  • 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: 113 SVs from 16 studies. See in: genome view    
Submitted genomic93,732,678-93,732,729Question Mark
Overlapping variant regions from other studies: 113 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):93,068,384-93,068,435Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5395648Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr593,732,67893,732,729
nsv5395648RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr593,068,38493,068,435

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16970400alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16970400Submitted genomicNC_000005.10:g.937
32678_93732729ins2
80
GRCh38 (hg38)NC_000005.10Chr593,732,67893,732,729
nssv16970400RemappedPerfectNC_000005.9:g.9306
8384_93068435ins28
0
GRCh37.p13First PassNC_000005.9Chr593,068,38493,068,435

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)
nssv169704000.00186404
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