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nsv5535915

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 143 SVs from 32 studies. See in: genome view    
Submitted genomic84,910,927-84,910,927Question Mark
Overlapping variant regions from other studies: 143 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):85,304,706-85,304,706Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5535915Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1284,910,92784,910,927
nsv5535915RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1285,304,70685,304,706

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17689728insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17689728Submitted genomicNC_000012.12:g.849
10927_84910928ins5
8
GRCh38 (hg38)NC_000012.12Chr1284,910,92784,910,927
nssv17689728RemappedPerfectNC_000012.11:g.853
04706_85304707ins5
8
GRCh37.p13First PassNC_000012.11Chr1285,304,70685,304,706

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)
nssv176897280.0523316400
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