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nsv5444670

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:173

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 148 SVs from 19 studies. See in: genome view    
Submitted genomic224,430,105-224,430,277Question Mark
Overlapping variant regions from other studies: 151 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):224,617,807-224,617,979Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5444670Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1224,430,105224,430,277
nsv5444670RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1224,617,807224,617,979

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16897224deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16897224Submitted genomicNC_000001.11:g.224
430105_224430277de
l
GRCh38 (hg38)NC_000001.11Chr1224,430,105224,430,277
nssv16897224RemappedPerfectNC_000001.10:g.224
617807_224617979de
l
GRCh37.p13First PassNC_000001.10Chr1224,617,807224,617,979

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)
nssv16897224<0.00126404
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