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nsv5548781

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 112 SVs from 13 studies. See in: genome view    
Submitted genomic171,333,048-171,333,061Question Mark
Overlapping variant regions from other studies: 112 SVs from 13 studies. See in: genome view    
Remapped(Score: Perfect):172,189,558-172,189,571Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5548781Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2171,333,048171,333,061
nsv5548781RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2172,189,558172,189,571

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16926833insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16926833Submitted genomicNC_000002.12:g.171
333048_171333061in
s50
GRCh38 (hg38)NC_000002.12Chr2171,333,048171,333,061
nssv16926833RemappedPerfectNC_000002.11:g.172
189558_172189571in
s50
GRCh37.p13First PassNC_000002.11Chr2172,189,558172,189,571

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)
nssv169268330.0342096178
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