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nsv5499690

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,794

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 83 SVs from 23 studies. See in: genome view    
Submitted genomic112,043,870-112,047,663Question Mark
Overlapping variant regions from other studies: 83 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):112,481,674-112,485,467Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5499690Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12112,043,870112,047,663
nsv5499690RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12112,481,674112,485,467

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17684531deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17684531Submitted genomicNC_000012.12:g.112
043870_112047663de
l
GRCh38 (hg38)NC_000012.12Chr12112,043,870112,047,663
nssv17684531RemappedPerfectNC_000012.11:g.112
481674_112485467de
l
GRCh37.p13First PassNC_000012.11Chr12112,481,674112,485,467

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)
nssv17684531<0.00116404
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