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nsv5439539

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:56

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 103 SVs from 20 studies. See in: genome view    
Submitted genomic210,027,874-210,027,929Question Mark
Overlapping variant regions from other studies: 103 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):210,892,598-210,892,653Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5439539Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2210,027,874210,027,929
nsv5439539RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2210,892,598210,892,653

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16924821duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16924821Submitted genomicNC_000002.12:g.210
027874_210027929du
p
GRCh38 (hg38)NC_000002.12Chr2210,027,874210,027,929
nssv16924821RemappedPerfectNC_000002.11:g.210
892598_210892653du
p
GRCh37.p13First PassNC_000002.11Chr2210,892,598210,892,653

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)
nssv16924821<0.00116404
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