esv5452

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:842

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 138 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):174,225,646-174,226,487Question Mark
Overlapping variant regions from other studies: 138 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):175,090,374-175,091,215Question Mark
Overlapping variant regions from other studies: 64 SVs from 12 studies. See in: genome view    
Submitted genomic174,798,620-174,799,461Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv5452RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000002.12Chr2174,225,646174,225,914174,226,215174,226,487
esv5452RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000002.11Chr2175,090,374175,090,642175,090,943175,091,215
esv5452Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000002.10Chr2174,798,620174,798,888174,799,189174,799,461

Variant Call Information

Variant Call IDTypeMethodAnalysis
essv27893copy number lossSequencingRead depth and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv27893RemappedPerfectNC_000002.12:g.(17
4225646_174225914)
_(174226215_174226
487)del
GRCh38 (hg38)First PassNC_000002.12Chr2174,225,646174,225,914174,226,215174,226,487
essv27893RemappedPerfectNC_000002.11:g.(17
5090374_175090642)
_(175090943_175091
215)del
GRCh37 (hg19)First PassNC_000002.11Chr2175,090,374175,090,642175,090,943175,091,215
essv27893Submitted genomicNC_000002.10:g.(17
4798620_174798888)
_(174799189_174799
461)del
NCBI36 (hg18)NC_000002.10Chr2174,798,620174,798,888174,799,189174,799,461

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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