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nsv5444907

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:287

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 151 SVs from 50 studies. See in: genome view    
Submitted genomic190,572,861-190,573,147Question Mark
Overlapping variant regions from other studies: 151 SVs from 50 studies. See in: genome view    
Remapped(Score: Perfect):190,290,650-190,290,936Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5444907Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3190,572,861190,573,147
nsv5444907RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3190,290,650190,290,936

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16944088deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16944088Submitted genomicNC_000003.12:g.190
572861_190573147de
l
GRCh38 (hg38)NC_000003.12Chr3190,572,861190,573,147
nssv16944088RemappedPerfectNC_000003.11:g.190
290650_190290936de
l
GRCh37.p13First PassNC_000003.11Chr3190,290,650190,290,936

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)
nssv169440880.35923016404
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