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nsv5552910

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:43

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 164 SVs from 14 studies. See in: genome view    
Submitted genomic16,576,842-16,576,884Question Mark
Overlapping variant regions from other studies: 164 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):16,576,951-16,576,993Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5552910Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr516,576,84216,576,884
nsv5552910RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr516,576,95116,576,993

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16962865insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16962865Submitted genomicNC_000005.10:g.165
76842_16576884ins3
06
GRCh38 (hg38)NC_000005.10Chr516,576,84216,576,884
nssv16962865RemappedPerfectNC_000005.9:g.1657
6951_16576993ins30
6
GRCh37.p13First PassNC_000005.9Chr516,576,95116,576,993

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)
nssv16962865<0.00116404
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