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nsv5443035

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:76

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 93 SVs from 15 studies. See in: genome view    
Submitted genomic218,238,797-218,238,872Question Mark
Overlapping variant regions from other studies: 93 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):219,103,520-219,103,595Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5443035Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2218,238,797218,238,872
nsv5443035RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2219,103,520219,103,595

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16928200duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16928200Submitted genomicNC_000002.12:g.218
238797_218238872du
p
GRCh38 (hg38)NC_000002.12Chr2218,238,797218,238,872
nssv16928200RemappedPerfectNC_000002.11:g.219
103520_219103595du
p
GRCh37.p13First PassNC_000002.11Chr2219,103,520219,103,595

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)
nssv16928200<0.00116404
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