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nsv4684415

  • Variant Calls:4
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,495,080

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 3709 SVs from 111 studies. See in: genome view    
Submitted genomic146,330,583-147,825,662Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeAssemblyAssembly UnitSequence IDChrInner StartInner Stop
nsv4684415Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1146,330,583147,825,662

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysis
nssv16215351deletionmb1:o2SNP arraySNP genotyping analysis
nssv16215354duplicationmb1:o7SNP arraySNP genotyping analysis
nssv16215355deletionmb1:o3SNP arraySNP genotyping analysis
nssv16215356deletionmb1:o4SNP arraySNP genotyping analysis

Variant Call Placement Information

Variant Call IDPlacement TypeHGVSAssemblySequence IDChrInner StartInner Stop
nssv16215351Submitted genomicNC_000001.10:g.(?_
146330583)_(147825
662_?)del
GRCh37 (hg19)NC_000001.10Chr1146,330,583147,825,662
nssv16215354Submitted genomicNC_000001.10:g.(?_
146330583)_(147825
662_?)dup
GRCh37 (hg19)NC_000001.10Chr1146,330,583147,825,662
nssv16215355Submitted genomicNC_000001.10:g.(?_
146330583)_(147825
662_?)del
GRCh37 (hg19)NC_000001.10Chr1146,330,583147,825,662
nssv16215356Submitted genomicNC_000001.10:g.(?_
146330583)_(147825
662_?)del
GRCh37 (hg19)NC_000001.10Chr1146,330,583147,825,662

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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