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esv1815923

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:187,410

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 883 SVs from 90 studies. See in: genome view    
Remapped(Score: Perfect):167,888,672-168,076,081Question Mark
Overlapping variant regions from other studies: 883 SVs from 90 studies. See in: genome view    
Remapped(Score: Perfect):168,809,823-168,997,232Question Mark
Overlapping variant regions from other studies: 281 SVs from 29 studies. See in: genome view    
Submitted genomic169,046,398-169,233,807Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner StopOuter Stop
esv1815923RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr4167,888,672168,070,673168,076,081
esv1815923RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4168,809,823168,991,824168,997,232
esv1815923Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000004.10Chr4169,046,398169,228,399169,233,807

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv4421540copy number gainNA18576Oligo aCGHProbe signal intensity9,809

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner StopOuter Stop
essv4421540RemappedPerfectNC_000004.12:g.(?_
167888672)_(168070
673_168076081)dup
GRCh38.p12First PassNC_000004.12Chr4167,888,672168,070,673168,076,081
essv4421540RemappedPerfectNC_000004.11:g.(?_
168809823)_(168991
824_168997232)dup
GRCh37.p13First PassNC_000004.11Chr4168,809,823168,991,824168,997,232
essv4421540Submitted genomicNC_000004.10:g.(?_
169046398)_(169228
399_169233807)dup
NCBI36 (hg18)NC_000004.10Chr4169,046,398169,228,399169,233,807

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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