esv5438

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,677

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 344 SVs from 49 studies. See in: genome view    
Remapped(Score: Perfect):189,136,618-189,143,294Question Mark
Overlapping variant regions from other studies: 344 SVs from 49 studies. See in: genome view    
Remapped(Score: Perfect):190,057,772-190,064,448Question Mark
Overlapping variant regions from other studies: 281 SVs from 20 studies. See in: genome view    
Submitted genomic190,294,766-190,301,442Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv5438RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000004.12Chr4189,136,618189,136,851189,143,120189,143,294
esv5438RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000004.11Chr4190,057,772190,058,005190,064,274190,064,448
esv5438Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000004.10Chr4190,294,766190,294,999190,301,268190,301,442

Variant Call Information

Variant Call IDTypeMethodAnalysis
essv27879copy number lossSequencingRead depth and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv27879RemappedPerfectNC_000004.12:g.(18
9136618_189136851)
_(189143120_189143
294)del
GRCh38 (hg38)First PassNC_000004.12Chr4189,136,618189,136,851189,143,120189,143,294
essv27879RemappedPerfectNC_000004.11:g.(19
0057772_190058005)
_(190064274_190064
448)del
GRCh37 (hg19)First PassNC_000004.11Chr4190,057,772190,058,005190,064,274190,064,448
essv27879Submitted genomicNC_000004.10:g.(19
0294766_190294999)
_(190301268_190301
442)del
NCBI36 (hg18)NC_000004.10Chr4190,294,766190,294,999190,301,268190,301,442

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

Support Center