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nsv5402888

  • 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: 121 SVs from 20 studies. See in: genome view    
Submitted genomic202,963,439-202,963,490Question Mark
Overlapping variant regions from other studies: 121 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):202,932,567-202,932,618Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5402888Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1202,963,439202,963,490
nsv5402888RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1202,932,567202,932,618

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16894846alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16894846Submitted genomicNC_000001.11:g.202
963439_202963490in
s280
GRCh38 (hg38)NC_000001.11Chr1202,963,439202,963,490
nssv16894846RemappedPerfectNC_000001.10:g.202
932567_202932618in
s280
GRCh37.p13First PassNC_000001.10Chr1202,932,567202,932,618

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)
nssv16894846<0.00126404
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