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esv2756804

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:205,408

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2133 SVs from 94 studies. See in: genome view    
Remapped(Score: Perfect):111,416,207-111,621,614Question Mark
Overlapping variant regions from other studies: 2133 SVs from 94 studies. See in: genome view    
Remapped(Score: Perfect):111,056,263-111,261,670Question Mark
Overlapping variant regions from other studies: 46 SVs from 10 studies. See in: genome view    
Submitted genomic110,650,214-110,855,621Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2756804RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7111,416,207111,621,614
esv2756804RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7111,056,263111,261,670
esv2756804Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000007.11Chr7110,650,214110,855,621

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv933copy number lossNA18949SNP arraySNP genotyping analysis133

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv933RemappedPerfectNC_000007.14:g.(11
1416207_111473535)
_(111590762_111621
614)del
GRCh38.p12First PassNC_000007.14Chr7111,416,207111,473,535111,590,762111,621,614
essv933RemappedPerfectNC_000007.13:g.(11
1056263_111113591)
_(111230818_111261
670)del
GRCh37.p13First PassNC_000007.13Chr7111,056,263111,113,591111,230,818111,261,670
essv933Submitted genomicNC_000007.11:g.(11
0650214_110707542)
_(110824769_110855
621)del
NCBI35 (hg17)NC_000007.11Chr7110,650,214110,707,542110,824,769110,855,621

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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