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nsv5539221

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:36

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 167 SVs from 39 studies. See in: genome view    
Submitted genomic109,921,269-109,921,304Question Mark
Overlapping variant regions from other studies: 167 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):110,842,425-110,842,460Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5539221Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4109,921,269109,921,304
nsv5539221RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4110,842,425110,842,460

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16954918insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16954918Submitted genomicNC_000004.12:g.109
921269_109921304in
s643
GRCh38 (hg38)NC_000004.12Chr4109,921,269109,921,304
nssv16954918RemappedPerfectNC_000004.11:g.110
842425_110842460in
s643
GRCh37.p13First PassNC_000004.11Chr4110,842,425110,842,460

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)
nssv169549180.011706404
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