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nsv5552585

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:51

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 143 SVs from 22 studies. See in: genome view    
Submitted genomic186,912,656-186,912,706Question Mark
Overlapping variant regions from other studies: 143 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):186,881,788-186,881,838Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5552585Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1186,912,656186,912,706
nsv5552585RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1186,881,788186,881,838

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16893235insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16893235Submitted genomicNC_000001.11:g.186
912656_186912706in
s68
GRCh38 (hg38)NC_000001.11Chr1186,912,656186,912,706
nssv16893235RemappedPerfectNC_000001.10:g.186
881788_186881838in
s68
GRCh37.p13First PassNC_000001.10Chr1186,881,788186,881,838

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)
nssv168932350.0975615766
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