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nsv5448061

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,077

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 147 SVs from 33 studies. See in: genome view    
Submitted genomic160,015,709-160,021,785Question Mark
Overlapping variant regions from other studies: 147 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):160,872,220-160,878,296Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5448061Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2160,015,709160,021,785
nsv5448061RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2160,872,220160,878,296

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16920212deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16920212Submitted genomicNC_000002.12:g.160
015709_160021785de
l
GRCh38 (hg38)NC_000002.12Chr2160,015,709160,021,785
nssv16920212RemappedPerfectNC_000002.11:g.160
872220_160878296de
l
GRCh37.p13First PassNC_000002.11Chr2160,872,220160,878,296

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)
nssv16920212<0.00126404
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