nsv5403962

  • 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: 153 SVs from 26 studies. See in: genome view    
Submitted genomic223,800,197-223,800,248Question Mark
Overlapping variant regions from other studies: 156 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):223,987,899-223,987,950Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5403962Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1223,800,197223,800,248
nsv5403962RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1223,987,899223,987,950

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16896031alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16896031Submitted genomicNC_000001.11:g.223
800197_223800248in
s281
GRCh38 (hg38)NC_000001.11Chr1223,800,197223,800,248
nssv16896031RemappedPerfectNC_000001.10:g.223
987899_223987950in
s281
GRCh37.p13First PassNC_000001.10Chr1223,987,899223,987,950

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)
nssv168960310.005346396
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