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nsv5444636

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,998,597

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 5350 SVs from 110 studies. See in: genome view    
Submitted genomic150,863,589-152,862,185Question Mark
Overlapping variant regions from other studies: 5350 SVs from 110 studies. See in: genome view    
Remapped(Score: Perfect):151,720,103-153,718,699Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5444636Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2150,863,589152,862,185
nsv5444636RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2151,720,103153,718,699

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16920925deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16920925Submitted genomicNC_000002.12:g.150
863589_152862185de
l
GRCh38 (hg38)NC_000002.12Chr2150,863,589152,862,185
nssv16920925RemappedPerfectNC_000002.11:g.151
720103_153718699de
l
GRCh37.p13First PassNC_000002.11Chr2151,720,103153,718,699

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)
nssv16920925<0.00116404
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