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nsv5892410

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:85,118

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2761 SVs from 105 studies. See in: genome view    
Submitted genomic31,268,945-31,354,062Question Mark
Overlapping variant regions from other studies: 2761 SVs from 105 studies. See in: genome view    
Remapped(Score: Perfect):31,236,722-31,321,839Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5892410Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr631,268,94531,354,062
nsv5892410RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr631,236,72231,321,839

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17435175duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17435175Submitted genomicNC_000006.12:g.312
68945_31354062dup
GRCh38 (hg38)NC_000006.12Chr631,268,94531,354,062
nssv17435175RemappedPerfectNC_000006.11:g.312
36722_31321839dup
GRCh37.p13First PassNC_000006.11Chr631,236,72231,321,839

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)
nssv174351750.2250228
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