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nsv5343131

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 115 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):232,765,663-232,765,663Question Mark
Overlapping variant regions from other studies: 1617 SVs from 78 studies. See in: genome view    
Remapped(Score: Perfect):32,534,146-32,534,146Question Mark
Overlapping variant regions from other studies: 115 SVs from 14 studies. See in: genome view    
Submitted genomic233,630,373-233,630,373Question Mark
Overlapping variant regions from other studies: 1617 SVs from 78 studies. See in: genome view    
Submitted genomic32,501,923-32,501,923Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
nsv5343131RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2232,765,663232,765,663-
nsv5343131RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr632,534,14632,534,146-
nsv5343131Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2233,630,373233,630,373-
nsv5343131Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr632,501,92332,501,923-

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16413563interchromosomal translocationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
nssv16413563RemappedPerfectGRCh38.p12First PassNC_000002.12Chr2232,765,663232,765,663-
nssv16413563RemappedPerfectGRCh38.p12First PassNC_000006.12Chr632,534,14632,534,146-
nssv16413563Submitted genomicGRCh37 (hg19)NC_000002.11Chr2233,630,373233,630,373-
nssv16413563Submitted genomicGRCh37 (hg19)NC_000006.11Chr632,501,92332,501,923-

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)
nssv164135630.199335316834
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