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nsv5535315

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:39

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 255 SVs from 28 studies. See in: genome view    
Submitted genomic184,653,664-184,653,702Question Mark
Overlapping variant regions from other studies: 255 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):185,574,818-185,574,856Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5535315Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4184,653,664184,653,702
nsv5535315RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4185,574,818185,574,856

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16962223insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16962223Submitted genomicNC_000004.12:g.184
653664_184653702in
s336
GRCh38 (hg38)NC_000004.12Chr4184,653,664184,653,702
nssv16962223RemappedPerfectNC_000004.11:g.185
574818_185574856in
s336
GRCh37.p13First PassNC_000004.11Chr4185,574,818185,574,856

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)
nssv169622230.002136404
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