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nsv4249713

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:103,030

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 135 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):11,240,808-11,343,837Question Mark
Overlapping variant regions from other studies: 135 SVs from 15 studies. See in: genome view    
Submitted genomic11,334,665-11,437,694Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4249713RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1611,240,80811,343,837
nsv4249713Submitted genomicGRCh37.p13Primary AssemblyNC_000016.9Chr1611,334,66511,437,694

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15954774duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15954774RemappedPerfectNC_000016.10:g.112
40808_11343837dup
GRCh38.p12First PassNC_000016.10Chr1611,240,80811,343,837
nssv15954774Submitted genomicNC_000016.9:g.1133
4665_11437694dup
GRCh37.p13NC_000016.9Chr1611,334,66511,437,694

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)
nssv159547744.6e-005121694
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