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nsv5941770

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:78,485

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1301 SVs from 95 studies. See in: genome view    
Submitted genomic14,964,786-15,043,270Question Mark
Overlapping variant regions from other studies: 1301 SVs from 95 studies. See in: genome view    
Remapped(Score: Perfect):15,058,643-15,137,127Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5941770Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1614,964,78615,043,270
nsv5941770RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1615,058,64315,137,127

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17380277duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17380277Submitted genomicNC_000016.10:g.149
64786_15043270dup
GRCh38 (hg38)NC_000016.10Chr1614,964,78615,043,270
nssv17380277RemappedPerfectNC_000016.9:g.1505
8643_15137127dup
GRCh37.p13First PassNC_000016.9Chr1615,058,64315,137,127

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)
nssv173802770.00341162
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