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nsv5408104

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 104 SVs from 22 studies. See in: genome view    
Submitted genomic77,039,428-77,039,479Question Mark
Overlapping variant regions from other studies: 104 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):76,335,253-76,335,304Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5408104Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr577,039,42877,039,479
nsv5408104RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr576,335,25376,335,304

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16968434alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16968434Submitted genomicNC_000005.10:g.770
39428_77039479ins2
38
GRCh38 (hg38)NC_000005.10Chr577,039,42877,039,479
nssv16968434RemappedPerfectNC_000005.9:g.7633
5253_76335304ins23
8
GRCh37.p13First PassNC_000005.9Chr576,335,25376,335,304

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)
nssv16968434<0.00116404
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