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nsv4712411

  • 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: 395 SVs from 57 studies. See in: genome view    
Remapped(Score: Perfect):63,832,084-63,832,084Question Mark
Overlapping variant regions from other studies: 188 SVs from 45 studies. See in: genome view    
Remapped(Score: Perfect):30,399,290-30,399,290Question Mark
Overlapping variant regions from other studies: 256 SVs from 52 studies. See in: genome view    
Submitted genomic68,427,818-68,427,818Question Mark
Overlapping variant regions from other studies: 153 SVs from 36 studies. See in: genome view    
Submitted genomic29,633,966-29,633,966Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
nsv4712411RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr963,832,08463,832,084-
nsv4712411RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2030,399,29030,399,290-
nsv4712411Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr968,427,81868,427,818-
nsv4712411Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000020.10Chr2029,633,96629,633,966-

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
nssv16252120interchromosomal translocationB450SequencingPaired-end mapping14,473

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
nssv16252120RemappedPerfectGRCh38.p12First PassNC_000009.12Chr963,832,08463,832,084-
nssv16252120RemappedPerfectGRCh38.p12First PassNC_000020.11Chr2030,399,29030,399,290-
nssv16252120Submitted genomicGRCh37 (hg19)NC_000009.11Chr968,427,81868,427,818-
nssv16252120Submitted genomicGRCh37 (hg19)NC_000020.10Chr2029,633,96629,633,966-

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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