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nsv4772221

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:930,000

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2355 SVs from 88 studies. See in: genome view    
Remapped(Score: Perfect):19,608,177-20,538,176Question Mark
Overlapping variant regions from other studies: 2355 SVs from 88 studies. See in: genome view    
Submitted genomic19,934,671-20,864,669Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4772221RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr119,608,17720,538,176
nsv4772221Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr119,934,67120,864,669

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16384283duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16384283RemappedPerfectNC_000001.11:g.196
08177_20538176dup
GRCh38.p12First PassNC_000001.11Chr119,608,17720,538,176
nssv16384283Submitted genomicNC_000001.10:g.199
34671_20864669dup
GRCh37 (hg19)NC_000001.10Chr119,934,67120,864,669

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)
nssv16384283<0.001116834
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