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nsv5563580

  • 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: 98 SVs from 26 studies. See in: genome view    
Submitted genomic52,596,348-52,596,399Question Mark
Overlapping variant regions from other studies: 98 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):52,990,132-52,990,183Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5563580Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1252,596,34852,596,399
nsv5563580RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1252,990,13252,990,183

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058783line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058783Submitted genomicNC_000012.12:g.525
96348_52596399ins6
019
GRCh38 (hg38)NC_000012.12Chr1252,596,34852,596,399
nssv17058783RemappedPerfectNC_000012.11:g.529
90132_52990183ins6
019
GRCh37.p13First PassNC_000012.11Chr1252,990,13252,990,183

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)
nssv17058783<0.00126404
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