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nsv4994360

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:350,668

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1349 SVs from 93 studies. See in: genome view    
Submitted genomic4,957,857-5,308,524Question Mark
Overlapping variant regions from other studies: 1349 SVs from 93 studies. See in: genome view    
Remapped(Score: Perfect):5,007,858-5,358,525Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4994360Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr164,957,8575,308,524
nsv4994360RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr165,007,8585,358,525

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16572121duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16572121Submitted genomicNC_000016.10:g.495
7857_5308524dup
GRCh38 (hg38)NC_000016.10Chr164,957,8575,308,524
nssv16572121RemappedPerfectNC_000016.9:g.5007
858_5358525dup
GRCh37.p13First PassNC_000016.9Chr165,007,8585,358,525

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)
nssv16572121<0.001129246
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