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nsv5399385

  • 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: 127 SVs from 23 studies. See in: genome view    
Submitted genomic119,458,843-119,458,894Question Mark
Overlapping variant regions from other studies: 127 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):118,794,538-118,794,589Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5399385Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5119,458,843119,458,894
nsv5399385RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5118,794,538118,794,589

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16973314alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16973314Submitted genomicNC_000005.10:g.119
458843_119458894in
s175
GRCh38 (hg38)NC_000005.10Chr5119,458,843119,458,894
nssv16973314RemappedPerfectNC_000005.9:g.1187
94538_118794589ins
175
GRCh37.p13First PassNC_000005.9Chr5118,794,538118,794,589

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)
nssv16973314<0.00166404
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