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nsv5471813

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,997

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 175 SVs from 41 studies. See in: genome view    
Submitted genomic109,919,584-109,924,580Question Mark
Overlapping variant regions from other studies: 175 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):110,840,740-110,845,736Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5471813Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4109,919,584109,924,580
nsv5471813RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4110,840,740110,845,736

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16954916deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16954916Submitted genomicNC_000004.12:g.109
919584_109924580de
l
GRCh38 (hg38)NC_000004.12Chr4109,919,584109,924,580
nssv16954916RemappedPerfectNC_000004.11:g.110
840740_110845736de
l
GRCh37.p13First PassNC_000004.11Chr4110,840,740110,845,736

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)
nssv169549160.015966404
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