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nsv3901163

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:17,020,312
  • Description:GRCh38/hg38 1p36.11-34.2(chr1:24381206-41401517)x3 AND See cases

Genome View

Select assembly:
Overlapping variant regions from other studies: 44828 SVs from 137 studies. See in: genome view    
Submitted genomic24,381,206-41,401,517Question Mark
Overlapping variant regions from other studies: 44852 SVs from 137 studies. See in: genome view    
Submitted genomic24,707,696-41,886,350Question Mark
Overlapping variant regions from other studies: 9828 SVs from 39 studies. See in: genome view    
Submitted genomic24,580,283-41,658,937Question Mark
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