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nsv6634295

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:443,136

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1040 SVs from 55 studies. See in: genome view    
Remapped(Score: Good):100,702,030-101,145,165Question Mark
Overlapping variant regions from other studies: 1041 SVs from 55 studies. See in: genome view    
Submitted genomic99,957,026-100,400,154Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv6634295RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX100,702,030101,145,165
nsv6634295Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000023.10ChrX99,957,026100,400,154

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv18283182duplicationOSC2286SNP arrayProbe signal intensity5

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv18283182RemappedGoodNC_000023.11:g.(?_
100702030)_(101145
165_?)dup
GRCh38.p12First PassNC_000023.11ChrX100,702,030101,145,165
nssv18283182Submitted genomicNC_000023.10:g.(?_
99957026)_(1004001
54_?)dup
GRCh37 (hg19)NC_000023.10ChrX99,957,026100,400,154

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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