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nsv5373276

  • 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: 80 SVs from 17 studies. See in: genome view    
Submitted genomic102,132,554-102,132,554Question Mark
Overlapping variant regions from other studies: 128 SVs from 23 studies. See in: genome view    
Submitted genomic112,293,160-112,293,160Question Mark
Overlapping variant regions from other studies: 80 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):103,892,311-103,892,311Question Mark
Overlapping variant regions from other studies: 128 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):114,052,918-114,052,918Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
nsv5373276Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10102,132,554102,132,554-
nsv5373276Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10112,293,160112,293,160-
nsv5373276RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10103,892,311103,892,311-
nsv5373276RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10114,052,918114,052,918-

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16535503intrachromosomal translocationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
nssv16535503Submitted genomicGRCh38 (hg38)NC_000010.11Chr10102,132,554102,132,554-
nssv16535503Submitted genomicGRCh38 (hg38)NC_000010.11Chr10112,293,160112,293,160-
nssv16535503RemappedPerfectGRCh37.p13First PassNC_000010.10Chr10103,892,311103,892,311-
nssv16535503RemappedPerfectGRCh37.p13First PassNC_000010.10Chr10114,052,918114,052,918-

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)
nssv16535503<0.001129246
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