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nsv5423473

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:695

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 114 SVs from 26 studies. See in: genome view    
Submitted genomic151,302,502-151,303,196Question Mark
Overlapping variant regions from other studies: 127 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):151,274,978-151,275,672Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5423473Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1151,302,502151,303,196
nsv5423473RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1151,274,978151,275,672

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16890273deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16890273Submitted genomicNC_000001.11:g.151
302502_151303196de
l
GRCh38 (hg38)NC_000001.11Chr1151,302,502151,303,196
nssv16890273RemappedPerfectNC_000001.10:g.151
274978_151275672de
l
GRCh37.p13First PassNC_000001.10Chr1151,274,978151,275,672

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)
nssv16890273<0.00156404
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