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nsv5396938

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:28

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 122 SVs from 21 studies. See in: genome view    
Submitted genomic202,961,490-202,961,517Question Mark
Overlapping variant regions from other studies: 122 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):202,930,618-202,930,645Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5396938Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1202,961,490202,961,517
nsv5396938RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1202,930,618202,930,645

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16894724alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16894724Submitted genomicNC_000001.11:g.202
961490_202961517in
s269
GRCh38 (hg38)NC_000001.11Chr1202,961,490202,961,517
nssv16894724RemappedPerfectNC_000001.10:g.202
930618_202930645in
s269
GRCh37.p13First PassNC_000001.10Chr1202,930,618202,930,645

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)
nssv16894724<0.00136404
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