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nsv5399456

  • 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: 133 SVs from 29 studies. See in: genome view    
Submitted genomic46,701,814-46,701,865Question Mark
Overlapping variant regions from other studies: 133 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):46,928,953-46,929,004Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5399456Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr246,701,81446,701,865
nsv5399456RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr246,928,95346,929,004

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16913664alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16913664Submitted genomicNC_000002.12:g.467
01814_46701865ins2
76
GRCh38 (hg38)NC_000002.12Chr246,701,81446,701,865
nssv16913664RemappedPerfectNC_000002.11:g.469
28953_46929004ins2
76
GRCh37.p13First PassNC_000002.11Chr246,928,95346,929,004

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)
nssv169136640.54634966404
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