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nsv5538563

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:24

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 181 SVs from 27 studies. See in: genome view    
Submitted genomic235,360,077-235,360,100Question Mark
Overlapping variant regions from other studies: 184 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):235,523,392-235,523,415Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5538563Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1235,360,077235,360,100
nsv5538563RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1235,523,392235,523,415

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16896574insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16896574Submitted genomicNC_000001.11:g.235
360077_235360100in
s114
GRCh38 (hg38)NC_000001.11Chr1235,360,077235,360,100
nssv16896574RemappedPerfectNC_000001.10:g.235
523392_235523415in
s114
GRCh37.p13First PassNC_000001.10Chr1235,523,392235,523,415

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)
nssv16896574<0.00126404
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