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nsv5424255

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:24,209

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 201 SVs from 41 studies. See in: genome view    
Submitted genomic113,699,005-113,723,213Question Mark
Overlapping variant regions from other studies: 202 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):114,241,627-114,265,835Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5424255Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1113,699,005113,723,213
nsv5424255RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1114,241,627114,265,835

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16889596deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16889596Submitted genomicNC_000001.11:g.113
699005_113723213de
l
GRCh38 (hg38)NC_000001.11Chr1113,699,005113,723,213
nssv16889596RemappedPerfectNC_000001.10:g.114
241627_114265835de
l
GRCh37.p13First PassNC_000001.10Chr1114,241,627114,265,835

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)
nssv16889596<0.00126404
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