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nsv4517069

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:650,002

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 206 SVs from 12 studies. See in: genome view    
Remapped(Score: Perfect):18,840,113-19,490,114Question Mark
Overlapping variant regions from other studies: 207 SVs from 12 studies. See in: genome view    
Submitted genomic21,001,999-21,652,000Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4517069RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000024.10ChrY18,840,11319,490,114
nsv4517069Submitted genomicGRCh37.p13Primary AssemblyNC_000024.9ChrY21,001,99921,652,000

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15990331duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15990331RemappedPerfectNC_000024.10:g.188
40113_19490114dup
GRCh38.p12First PassNC_000024.10ChrY18,840,11319,490,114
nssv15990331Submitted genomicNC_000024.9:g.2100
1999_21652000dup
GRCh37.p13NC_000024.9ChrY21,001,99921,652,000

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)
nssv15990331<0.001621694
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