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nsv5452774

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:556

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 170 SVs from 32 studies. See in: genome view    
Submitted genomic183,124,918-183,125,473Question Mark
Overlapping variant regions from other studies: 170 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):183,989,646-183,990,201Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5452774Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2183,124,918183,125,473
nsv5452774RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2183,989,646183,990,201

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16922665deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16922665Submitted genomicNC_000002.12:g.183
124918_183125473de
l
GRCh38 (hg38)NC_000002.12Chr2183,124,918183,125,473
nssv16922665RemappedPerfectNC_000002.11:g.183
989646_183990201de
l
GRCh37.p13First PassNC_000002.11Chr2183,989,646183,990,201

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)
nssv169226650.009576404
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