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nsv4201116

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:94,137

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 50 SVs from 14 studies. See in: genome view    
Remapped(Score: Good):77,020,671-77,114,807Question Mark
Overlapping variant regions from other studies: 47 SVs from 14 studies. See in: genome view    
Submitted genomic76,731,715-76,825,853Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4201116RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1177,020,67177,114,807
nsv4201116Submitted genomicGRCh37.p13Primary AssemblyNC_000011.9Chr1176,731,71576,825,853

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15953603duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15953603RemappedGoodNC_000011.10:g.770
20671_77114807dup
GRCh38.p12First PassNC_000011.10Chr1177,020,67177,114,807
nssv15953603Submitted genomicNC_000011.9:g.7673
1715_76825853dup
GRCh37.p13NC_000011.9Chr1176,731,71576,825,853

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv159536034.6e-005121694
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