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nsv5870847

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:118,427

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1084 SVs from 96 studies. See in: genome view    
Submitted genomic25,287,187-25,405,613Question Mark
Overlapping variant regions from other studies: 1084 SVs from 96 studies. See in: genome view    
Remapped(Score: Perfect):25,613,678-25,732,104Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5870847Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr125,287,18725,405,613
nsv5870847RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr125,613,67825,732,104

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17360228duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17360228Submitted genomicNC_000001.11:g.252
87187_25405613dup
GRCh38 (hg38)NC_000001.11Chr125,287,18725,405,613
nssv17360228RemappedPerfectNC_000001.10:g.256
13678_25732104dup
GRCh37.p13First PassNC_000001.10Chr125,613,67825,732,104

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)
nssv173602280.0419458
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