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nsv5548184

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:49

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 138 SVs from 29 studies. See in: genome view    
Submitted genomic74,095,356-74,095,404Question Mark
Overlapping variant regions from other studies: 138 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):74,961,073-74,961,121Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5548184Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr474,095,35674,095,404
nsv5548184RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr474,961,07374,961,121

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16952301insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16952301Submitted genomicNC_000004.12:g.740
95356_74095404ins8
4
GRCh38 (hg38)NC_000004.12Chr474,095,35674,095,404
nssv16952301RemappedPerfectNC_000004.11:g.749
61073_74961121ins8
4
GRCh37.p13First PassNC_000004.11Chr474,961,07374,961,121

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)
nssv16952301<0.00116404
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