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nsv5009149

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:230,052

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 832 SVs from 69 studies. See in: genome view    
Submitted genomic88,891,164-89,121,215Question Mark
Overlapping variant regions from other studies: 832 SVs from 69 studies. See in: genome view    
Remapped(Score: Perfect):89,434,395-89,664,446Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5009149Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1588,891,16489,121,215
nsv5009149RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1589,434,39589,664,446

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16573929duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16573929Submitted genomicNC_000015.10:g.888
91164_89121215dup
GRCh38 (hg38)NC_000015.10Chr1588,891,16489,121,215
nssv16573929RemappedPerfectNC_000015.9:g.8943
4395_89664446dup
GRCh37.p13First PassNC_000015.9Chr1589,434,39589,664,446

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16573929<0.001129246
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